Canonical Allele Identifier: CA16616178
Gene: SMARCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 408657
ClinVar RCV Id: RCV000458006
dbSNP Id: rs1060502088

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11039495del , CM000681.2:g.11039495del GRCh38
NC_000019.9:g.11150171del , CM000681.1:g.11150171del GRCh37
NC_000019.8:g.11011171del NCBI36
NG_011556.2:g.83574del
NG_011556.3:g.83564del

Transcript Alleles

HGVS Amino-acid change
ENST00000711079.1:c.4208del ENSP00000518564.1:p.Ser1403MetfsTer?
ENST00000704344.1:c.4171-1812del ENSP00000515855.1:n.4171-1812del
ENST00000646693.2:c.4208del MANE Plus Clinical ENSP00000495368.1:p.Ser1403MetfsTer?
ENST00000344626.10:c.4171-1812del MANE Select ENSP00000343896.4:n.4171-1812del
ENST00000429416.8:c.4171-1812del ENSP00000395654.1:n.4171-1812del
ENST00000444061.8:c.4072-1812del ENSP00000392837.2:n.4072-1812del
ENST00000538456.4:c.329-1803del
ENST00000586985.2:c.298-1812del ENSP00000467796.2:n.298-1812del
ENST00000590574.6:c.4072-1812del ENSP00000466963.1:n.4072-1812del
ENST00000592158.2:c.112-1812del ENSP00000467200.2:n.112-1812del
ENST00000592604.6:n.2403-1803del
ENST00000642350.1:c.2656-1803del ENSP00000495355.1:n.2656-1803del
ENST00000642508.1:c.1569del
ENST00000642628.1:c.4109del ENSP00000496498.1:p.Ser1370MetfsTer?
ENST00000642726.1:c.4109del ENSP00000494353.1:p.Ser1370MetfsTer?
ENST00000643208.1:c.2728-1812del ENSP00000496074.1:n.2728-1812del
ENST00000643296.1:c.4072-1803del ENSP00000496635.1:n.4072-1803del
ENST00000643534.1:c.2456-1812del
ENST00000643549.1:c.4109del ENSP00000493975.1:p.Ser1370MetfsTer22
ENST00000643857.1:c.2526-1803del
ENST00000643995.1:c.3585-1803del
ENST00000644065.1:c.2799-1803del
ENST00000644267.1:n.2563del
ENST00000644327.1:c.2843-1812del
ENST00000644737.1:c.4072-1803del ENSP00000495548.1:n.4072-1803del
ENST00000644963.1:c.2816-1803del
ENST00000645061.1:c.2659-1812del ENSP00000493690.1:n.2659-1812del
ENST00000645236.1:c.720-1812del
ENST00000645460.1:c.4072-1812del ENSP00000494463.1:n.4072-1812del
ENST00000645648.1:c.2082-1812del ENSP00000493521.1:n.2082-1812del
ENST00000646183.1:c.2455del
ENST00000646236.1:c.1802del ENSP00000493925.1:n.1802del
ENST00000646484.1:c.4072-1812del ENSP00000495536.1:n.4072-1812del
ENST00000646510.1:c.4072-1812del ENSP00000494772.1:n.4072-1812del
ENST00000646593.1:c.2019-1812del ENSP00000494341.1:n.2019-1812del
ENST00000646693.1:c.4208del ENSP00000495368.1:p.Ser1403MetfsTer?
ENST00000646746.1:c.2471-1812del
ENST00000647230.1:c.4072-1812del ENSP00000494676.1:n.4072-1812del
ENST00000647268.1:c.2425-1812del ENSP00000496176.1:n.2425-1812del
ENST00000344626.8:c.4171-1812del ENSP00000343896.4:n.4171-1812del
ENST00000413806.7:c.4264-1803del ENSP00000414727.3:n.4264-1803del
ENST00000429416.7:c.4171-1812del ENSP00000395654.1:n.4171-1812del
ENST00000444061.7:c.4072-1812del ENSP00000392837.2:n.4072-1812del
ENST00000450717.7:c.4208del ENSP00000397783.3:p.Ser1403MetfsTer?
ENST00000538456.3:n.417del
ENST00000541122.6:c.4072-1803del ENSP00000445036.2:n.4072-1803del
ENST00000585799.5:n.2600-1803del
ENST00000589677.5:c.4072-1803del ENSP00000464778.1:n.4072-1803del
ENST00000590574.5:c.4072-1812del ENSP00000466963.1:n.4072-1812del
ENST00000591595.5:n.2144-1812del
ENST00000592158.1:c.241-1803del ENSP00000467200.1:n.241-1803del
ENST00000592604.5:n.1985-1803del
NM_001128844.1:c.4171-1812del NP_001122316.1:n.4171-1812del
NM_001128845.1:c.4072-1803del NP_001122317.1:n.4072-1803del
NM_001128846.1:c.4072-1803del NP_001122318.1:n.4072-1803del
NM_001128847.1:c.4072-1812del NP_001122319.1:n.4072-1812del
NM_001128848.1:c.4072-1812del NP_001122320.1:n.4072-1812del
NM_001128849.1:c.4208del NP_001122321.1:p.Ser1403MetfsTer?
NM_003072.3:c.4171-1812del NP_003063.2:n.4171-1812del
XM_005260028.2:c.4171-1803del XP_005260085.1:n.4171-1803del
XM_005260030.2:c.4109del XP_005260087.1:p.Ser1370MetfsTer?
XM_005260031.2:c.4171-1812del XP_005260088.1:n.4171-1812del
XM_005260032.2:c.4072-1803del XP_005260089.1:n.4072-1803del
XM_005260033.2:c.4072-1803del XP_005260090.1:n.4072-1803del
XM_005260034.2:c.4072-1812del XP_005260091.1:n.4072-1812del
XM_005260035.2:c.4072-1812del XP_005260092.1:n.4072-1812del
XM_006722845.2:c.4208del XP_006722908.1:p.Ser1403MetfsTer?
XM_006722846.2:c.4208del XP_006722909.1:p.Ser1403MetfsTer?
XM_006722847.2:c.4208del XP_006722910.1:p.Ser1403MetfsTer?
XM_011528198.1:c.4208del XP_011526500.1:p.Ser1403MetfsTer?
XM_024451658.1:c.4208del XP_024307426.1:p.Ser1403MetfsTer?
XM_024451659.1:c.4208del XP_024307427.1:p.Ser1403MetfsTer?
XM_024451660.1:c.4171-1803del XP_024307428.1:n.4171-1803del
XM_024451661.1:c.4109del XP_024307429.1:p.Ser1370MetfsTer?
XM_024451662.1:c.4171-1812del XP_024307430.1:n.4171-1812del
XM_024451663.1:c.4109del XP_024307431.1:p.Ser1370MetfsTer?
XM_024451664.1:c.4072-1803del XP_024307432.1:n.4072-1803del
XM_024451665.1:c.4072-1803del XP_024307433.1:n.4072-1803del
XM_024451666.1:c.4072-1812del XP_024307434.1:n.4072-1812del
XM_024451667.1:c.4072-1812del XP_024307435.1:n.4072-1812del
NM_001128844.3:c.4171-1812del NP_001122316.1:n.4171-1812del
NM_001128845.2:c.4072-1803del NP_001122317.1:n.4072-1803del
NM_001128846.2:c.4072-1803del NP_001122318.1:n.4072-1803del
NM_001128847.4:c.4072-1812del NP_001122319.1:n.4072-1812del
NM_001128848.2:c.4072-1812del NP_001122320.1:n.4072-1812del
NM_001128849.3:c.4208del NP_001122321.1:p.Ser1403MetfsTer?
NM_001374457.1:c.4072-1812del NP_001361386.1:n.4072-1812del
NM_003072.5:c.4171-1812del MANE Select NP_003063.2:n.4171-1812del
NR_164683.1:n.4362-206del
NM_001387283.1:c.4208del MANE Plus Clinical NP_001374212.1:p.Ser1403MetfsTer?