Canonical Allele Identifier: CA404065107
Gene: SMARCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 426308
ClinVar RCV Id: RCV000490168
dbSNP Id: rs1085307556

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11033299G>A , CM000681.2:g.11033299G>A GRCh38
NC_000019.9:g.11143975G>A , CM000681.1:g.11143975G>A GRCh37
NC_000019.8:g.11004975G>A NCBI36
NG_011556.2:g.77378G>A
NG_011556.3:g.77368G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000711079.1:c.3556G>A ENSP00000518564.1:p.Ala1186Thr
ENST00000704344.1:c.3556G>A ENSP00000515855.1:p.Ala1186Thr
ENST00000704345.1:c.3547G>A ENSP00000515856.1:p.Ala1183Thr
ENST00000646693.2:c.3556G>A MANE Plus Clinical ENSP00000495368.1:p.Ala1186Thr
ENST00000344626.10:c.3556G>A MANE Select ENSP00000343896.4:p.Ala1186Thr
ENST00000429416.8:c.3556G>A ENSP00000395654.1:p.Ala1186Thr
ENST00000444061.8:c.3556G>A ENSP00000392837.2:p.Ala1186Thr
ENST00000590574.6:c.3556G>A ENSP00000466963.1:p.Ala1186Thr
ENST00000592604.6:n.1887G>A
ENST00000642350.1:c.2041G>A ENSP00000495355.1:p.Ala681Thr
ENST00000642508.1:c.917G>A
ENST00000642628.1:c.3556G>A ENSP00000496498.1:p.Ala1186Thr
ENST00000642726.1:c.3556G>A ENSP00000494353.1:p.Ala1186Thr
ENST00000643208.1:c.2113G>A ENSP00000496074.1:p.Ala705Thr
ENST00000643296.1:c.3556G>A ENSP00000496635.1:p.Ala1186Thr
ENST00000643534.1:c.1841G>A
ENST00000643549.1:c.3556G>A ENSP00000493975.1:p.Ala1186Thr
ENST00000643857.1:c.1911G>A
ENST00000643995.1:c.2970G>A
ENST00000644065.1:c.2283G>A
ENST00000644267.1:n.1911G>A
ENST00000644327.1:c.2327G>A
ENST00000644737.1:c.3556G>A ENSP00000495548.1:p.Ala1186Thr
ENST00000644963.1:c.2201G>A
ENST00000645061.1:c.2044G>A ENSP00000493690.1:p.Ala682Thr
ENST00000645236.1:c.105G>A
ENST00000645460.1:c.3556G>A ENSP00000494463.1:p.Ala1186Thr
ENST00000645648.1:c.1472G>A ENSP00000493521.1:n.1472G>A
ENST00000646183.1:c.1902G>A
ENST00000646236.1:c.1150G>A ENSP00000493925.1:n.1150G>A
ENST00000646484.1:c.3556G>A ENSP00000495536.1:p.Ala1186Thr
ENST00000646510.1:c.3556G>A ENSP00000494772.1:p.Ala1186Thr
ENST00000646593.1:c.1404G>A ENSP00000494341.1:n.1404G>A
ENST00000646693.1:c.3556G>A ENSP00000495368.1:p.Ala1186Thr
ENST00000646746.1:c.1856G>A
ENST00000647230.1:c.3556G>A ENSP00000494676.1:p.Ala1186Thr
ENST00000647268.1:c.1909G>A ENSP00000496176.1:p.Ala637Thr
ENST00000344626.8:c.3556G>A ENSP00000343896.4:p.Ala1186Thr
ENST00000413806.7:c.3748G>A ENSP00000414727.3:p.Ala1250Thr
ENST00000429416.7:c.3556G>A ENSP00000395654.1:p.Ala1186Thr
ENST00000444061.7:c.3556G>A ENSP00000392837.2:p.Ala1186Thr
ENST00000450717.7:c.3556G>A ENSP00000397783.3:p.Ala1186Thr
ENST00000541122.6:c.3556G>A ENSP00000445036.2:p.Ala1186Thr
ENST00000585799.5:n.2084G>A
ENST00000586892.1:n.218G>A
ENST00000589677.5:c.3556G>A ENSP00000464778.1:p.Ala1186Thr
ENST00000590574.5:c.3556G>A ENSP00000466963.1:p.Ala1186Thr
ENST00000591595.5:n.1628G>A
ENST00000592158.1:c.91G>A ENSP00000467200.1:p.Ala31Thr
ENST00000592604.5:n.1469G>A
NM_001128844.1:c.3556G>A NP_001122316.1:p.Ala1186Thr
NM_001128845.1:c.3556G>A NP_001122317.1:p.Ala1186Thr
NM_001128846.1:c.3556G>A NP_001122318.1:p.Ala1186Thr
NM_001128847.1:c.3556G>A NP_001122319.1:p.Ala1186Thr
NM_001128848.1:c.3556G>A NP_001122320.1:p.Ala1186Thr
NM_001128849.1:c.3556G>A NP_001122321.1:p.Ala1186Thr
NM_003072.3:c.3556G>A NP_003063.2:p.Ala1186Thr
XM_005260028.2:c.3556G>A XP_005260085.1:p.Ala1186Thr
XM_005260030.2:c.3556G>A XP_005260087.1:p.Ala1186Thr
XM_005260031.2:c.3556G>A XP_005260088.1:p.Ala1186Thr
XM_005260032.2:c.3556G>A XP_005260089.1:p.Ala1186Thr
XM_005260033.2:c.3556G>A XP_005260090.1:p.Ala1186Thr
XM_005260034.2:c.3556G>A XP_005260091.1:p.Ala1186Thr
XM_005260035.2:c.3556G>A XP_005260092.1:p.Ala1186Thr
XM_006722845.2:c.3556G>A XP_006722908.1:p.Ala1186Thr
XM_006722846.2:c.3556G>A XP_006722909.1:p.Ala1186Thr
XM_006722847.2:c.3556G>A XP_006722910.1:p.Ala1186Thr
XM_011528198.1:c.3556G>A XP_011526500.1:p.Ala1186Thr
XM_024451658.1:c.3556G>A XP_024307426.1:p.Ala1186Thr
XM_024451659.1:c.3556G>A XP_024307427.1:p.Ala1186Thr
XM_024451660.1:c.3556G>A XP_024307428.1:p.Ala1186Thr
XM_024451661.1:c.3556G>A XP_024307429.1:p.Ala1186Thr
XM_024451662.1:c.3556G>A XP_024307430.1:p.Ala1186Thr
XM_024451663.1:c.3556G>A XP_024307431.1:p.Ala1186Thr
XM_024451664.1:c.3556G>A XP_024307432.1:p.Ala1186Thr
XM_024451665.1:c.3556G>A XP_024307433.1:p.Ala1186Thr
XM_024451666.1:c.3556G>A XP_024307434.1:p.Ala1186Thr
XM_024451667.1:c.3556G>A XP_024307435.1:p.Ala1186Thr
NM_001128844.3:c.3556G>A NP_001122316.1:p.Ala1186Thr
NM_001128845.2:c.3556G>A NP_001122317.1:p.Ala1186Thr
NM_001128846.2:c.3556G>A NP_001122318.1:p.Ala1186Thr
NM_001128847.4:c.3556G>A NP_001122319.1:p.Ala1186Thr
NM_001128848.2:c.3556G>A NP_001122320.1:p.Ala1186Thr
NM_001128849.3:c.3556G>A NP_001122321.1:p.Ala1186Thr
NM_001374457.1:c.3556G>A NP_001361386.1:p.Ala1186Thr
NM_003072.5:c.3556G>A MANE Select NP_003063.2:p.Ala1186Thr
NR_164683.1:n.3846G>A
NM_001387283.1:c.3556G>A MANE Plus Clinical NP_001374212.1:p.Ala1186Thr