Canonical Allele Identifier: CA16616145
Gene: SMARCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 408702
ClinVar RCV Id: RCV000466062
dbSNP Id: rs1060502102

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11023517G>A , CM000681.2:g.11023517G>A GRCh38
NC_000019.9:g.11134193G>A , CM000681.1:g.11134193G>A GRCh37
NC_000019.8:g.10995193G>A NCBI36
NG_011556.2:g.67596G>A
NG_011556.3:g.67586G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000711079.1:c.2860-1G>A ENSP00000518564.1:n.2860-1G>A
ENST00000704344.1:c.2860-1G>A ENSP00000515855.1:n.2860-1G>A
ENST00000704345.1:c.2851-1G>A ENSP00000515856.1:n.2851-1G>A
ENST00000646693.2:c.2860-1G>A MANE Plus Clinical ENSP00000495368.1:n.2860-1G>A
ENST00000344626.10:c.2860-1G>A MANE Select ENSP00000343896.4:n.2860-1G>A
ENST00000429416.8:c.2860-1G>A ENSP00000395654.1:n.2860-1G>A
ENST00000444061.8:c.2860-1G>A ENSP00000392837.2:n.2860-1G>A
ENST00000590574.6:c.2860-1G>A ENSP00000466963.1:n.2860-1G>A
ENST00000591545.6:c.2733-1G>A
ENST00000592604.6:n.1191-1G>A
ENST00000642350.1:c.1345-1G>A ENSP00000495355.1:n.1345-1G>A
ENST00000642508.1:c.221-1G>A
ENST00000642628.1:c.2860-1G>A ENSP00000496498.1:n.2860-1G>A
ENST00000642726.1:c.2860-1G>A ENSP00000494353.1:n.2860-1G>A
ENST00000643208.1:c.1417-1G>A ENSP00000496074.1:n.1417-1G>A
ENST00000643296.1:c.2860-1G>A ENSP00000496635.1:n.2860-1G>A
ENST00000643534.1:c.1145-1G>A
ENST00000643549.1:c.2860-1G>A ENSP00000493975.1:n.2860-1G>A
ENST00000643857.1:c.1215-1G>A
ENST00000643995.1:c.2274-1G>A
ENST00000644065.1:c.1587-1G>A
ENST00000644267.1:n.1215-1G>A
ENST00000644290.1:c.1117-1G>A
ENST00000644327.1:c.1631-1G>A
ENST00000644737.1:c.2860-1G>A ENSP00000495548.1:n.2860-1G>A
ENST00000644963.1:c.1505-1G>A
ENST00000645061.1:c.1348-1G>A ENSP00000493690.1:n.1348-1G>A
ENST00000645460.1:c.2860-1G>A ENSP00000494463.1:n.2860-1G>A
ENST00000645648.1:c.724-1G>A ENSP00000493521.1:n.724-1G>A
ENST00000646183.1:c.1206-1G>A
ENST00000646236.1:c.343-1G>A ENSP00000493925.1:n.343-1G>A
ENST00000646484.1:c.2860-1G>A ENSP00000495536.1:n.2860-1G>A
ENST00000646510.1:c.2860-1G>A ENSP00000494772.1:n.2860-1G>A
ENST00000646513.1:c.694-1G>A ENSP00000495457.1:n.694-1G>A
ENST00000646593.1:c.708-1G>A ENSP00000494341.1:n.708-1G>A
ENST00000646693.1:c.2860-1G>A ENSP00000495368.1:n.2860-1G>A
ENST00000646746.1:c.1160-1G>A
ENST00000647230.1:c.2860-1G>A ENSP00000494676.1:n.2860-1G>A
ENST00000647268.1:c.1213-1G>A ENSP00000496176.1:n.1213-1G>A
ENST00000344626.8:c.2860-1G>A ENSP00000343896.4:n.2860-1G>A
ENST00000413806.7:c.3052-1G>A ENSP00000414727.3:n.3052-1G>A
ENST00000429416.7:c.2860-1G>A ENSP00000395654.1:n.2860-1G>A
ENST00000444061.7:c.2860-1G>A ENSP00000392837.2:n.2860-1G>A
ENST00000450717.7:c.2860-1G>A ENSP00000397783.3:n.2860-1G>A
ENST00000541122.6:c.2860-1G>A ENSP00000445036.2:n.2860-1G>A
ENST00000585799.5:n.1388-1G>A
ENST00000586122.5:n.442-1G>A
ENST00000587988.5:n.509-1G>A
ENST00000589677.5:c.2860-1G>A ENSP00000464778.1:n.2860-1G>A
ENST00000590574.5:c.2860-1G>A ENSP00000466963.1:n.2860-1G>A
ENST00000591545.5:n.2734-1G>A
ENST00000591595.5:n.932-1G>A
ENST00000592604.5:n.773-1G>A
NM_001128844.1:c.2860-1G>A NP_001122316.1:n.2860-1G>A
NM_001128845.1:c.2860-1G>A NP_001122317.1:n.2860-1G>A
NM_001128846.1:c.2860-1G>A NP_001122318.1:n.2860-1G>A
NM_001128847.1:c.2860-1G>A NP_001122319.1:n.2860-1G>A
NM_001128848.1:c.2860-1G>A NP_001122320.1:n.2860-1G>A
NM_001128849.1:c.2860-1G>A NP_001122321.1:n.2860-1G>A
NM_003072.3:c.2860-1G>A NP_003063.2:n.2860-1G>A
XM_005260028.2:c.2860-1G>A XP_005260085.1:n.2860-1G>A
XM_005260030.2:c.2860-1G>A XP_005260087.1:n.2860-1G>A
XM_005260031.2:c.2860-1G>A XP_005260088.1:n.2860-1G>A
XM_005260032.2:c.2860-1G>A XP_005260089.1:n.2860-1G>A
XM_005260033.2:c.2860-1G>A XP_005260090.1:n.2860-1G>A
XM_005260034.2:c.2860-1G>A XP_005260091.1:n.2860-1G>A
XM_005260035.2:c.2860-1G>A XP_005260092.1:n.2860-1G>A
XM_006722845.2:c.2860-1G>A XP_006722908.1:n.2860-1G>A
XM_006722846.2:c.2860-1G>A XP_006722909.1:n.2860-1G>A
XM_006722847.2:c.2860-1G>A XP_006722910.1:n.2860-1G>A
XM_011528198.1:c.2860-1G>A XP_011526500.1:n.2860-1G>A
XM_024451658.1:c.2860-1G>A XP_024307426.1:n.2860-1G>A
XM_024451659.1:c.2860-1G>A XP_024307427.1:n.2860-1G>A
XM_024451660.1:c.2860-1G>A XP_024307428.1:n.2860-1G>A
XM_024451661.1:c.2860-1G>A XP_024307429.1:n.2860-1G>A
XM_024451662.1:c.2860-1G>A XP_024307430.1:n.2860-1G>A
XM_024451663.1:c.2860-1G>A XP_024307431.1:n.2860-1G>A
XM_024451664.1:c.2860-1G>A XP_024307432.1:n.2860-1G>A
XM_024451665.1:c.2860-1G>A XP_024307433.1:n.2860-1G>A
XM_024451666.1:c.2860-1G>A XP_024307434.1:n.2860-1G>A
XM_024451667.1:c.2860-1G>A XP_024307435.1:n.2860-1G>A
NM_001128844.3:c.2860-1G>A NP_001122316.1:n.2860-1G>A
NM_001128845.2:c.2860-1G>A NP_001122317.1:n.2860-1G>A
NM_001128846.2:c.2860-1G>A NP_001122318.1:n.2860-1G>A
NM_001128847.4:c.2860-1G>A NP_001122319.1:n.2860-1G>A
NM_001128848.2:c.2860-1G>A NP_001122320.1:n.2860-1G>A
NM_001128849.3:c.2860-1G>A NP_001122321.1:n.2860-1G>A
NM_001374457.1:c.2860-1G>A NP_001361386.1:n.2860-1G>A
NM_003072.5:c.2860-1G>A MANE Select NP_003063.2:n.2860-1G>A
NR_164683.1:n.3150-1G>A
NM_001387283.1:c.2860-1G>A MANE Plus Clinical NP_001374212.1:n.2860-1G>A