Canonical Allele Identifier: CA2322734720
Gene: SMARCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11041349C= , CM000681.2:g.11041349C= GRCh38
NC_000019.9:g.11152025C= , CM000681.1:g.11152025C= GRCh37
NC_000019.8:g.11013025C= NCBI36
NG_011556.2:g.85428C=
NG_011556.3:g.85418C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000711079.1:c.4309C= ENSP00000518564.1:p.Arg1437=
ENST00000704344.1:c.4213C= ENSP00000515855.1:p.Arg1405=
ENST00000646693.2:c.4309C= MANE Plus Clinical ENSP00000495368.1:p.Arg1437=
ENST00000344626.10:c.4213C= MANE Select ENSP00000343896.4:p.Arg1405=
ENST00000429416.8:c.4213C= ENSP00000395654.1:p.Arg1405=
ENST00000444061.8:c.4114C= ENSP00000392837.2:p.Arg1372=
ENST00000538456.4:c.380C=
ENST00000586985.2:c.340C= ENSP00000467796.2:p.Arg114=
ENST00000590574.6:c.4114C= ENSP00000466963.1:p.Arg1372=
ENST00000592158.2:c.154C= ENSP00000467200.2:p.Arg52=
ENST00000592604.6:n.2454C=
ENST00000642350.1:c.2707C= ENSP00000495355.1:p.Arg903=
ENST00000642508.1:c.1670C=
ENST00000642628.1:c.4210C= ENSP00000496498.1:p.Arg1404=
ENST00000642726.1:c.4210C= ENSP00000494353.1:p.Arg1404=
ENST00000643208.1:c.2770C= ENSP00000496074.1:p.Arg924=
ENST00000643296.1:c.4123C= ENSP00000496635.1:p.Arg1375=
ENST00000643534.1:c.2498C=
ENST00000643549.1:c.4219C= ENSP00000493975.1:p.Arg1407=
ENST00000643857.1:c.2577C=
ENST00000643929.1:n.706C=
ENST00000643995.1:c.3636C=
ENST00000644065.1:c.2850C=
ENST00000644327.1:c.2885C=
ENST00000644737.1:c.4123C= ENSP00000495548.1:p.Arg1375=
ENST00000644963.1:c.2867C=
ENST00000645061.1:c.2701C= ENSP00000493690.1:p.Arg901=
ENST00000645236.1:c.762C=
ENST00000645460.1:c.4114C= ENSP00000494463.1:p.Arg1372=
ENST00000645648.1:c.2124C= ENSP00000493521.1:n.2124C=
ENST00000646183.1:c.2556C=
ENST00000646484.1:c.4114C= ENSP00000495536.1:p.Arg1372=
ENST00000646510.1:c.4114C= ENSP00000494772.1:p.Arg1372=
ENST00000646593.1:c.2061C= ENSP00000494341.1:n.2061C=
ENST00000646693.1:c.4309C= ENSP00000495368.1:p.Arg1437=
ENST00000646746.1:c.2513C=
ENST00000646889.1:n.716C=
ENST00000647230.1:c.4114C= ENSP00000494676.1:p.Arg1372=
ENST00000647268.1:c.2467C= ENSP00000496176.1:p.Arg823=
ENST00000344626.8:c.4213C= ENSP00000343896.4:p.Arg1405=
ENST00000413806.7:c.4315C= ENSP00000414727.3:p.Arg1439=
ENST00000429416.7:c.4213C= ENSP00000395654.1:p.Arg1405=
ENST00000444061.7:c.4114C= ENSP00000392837.2:p.Arg1372=
ENST00000450717.7:c.4309C= ENSP00000397783.3:p.Arg1437=
ENST00000538456.3:n.527C=
ENST00000541122.6:c.4123C= ENSP00000445036.2:p.Arg1375=
ENST00000585799.5:n.2651C=
ENST00000589677.5:c.4123C= ENSP00000464778.1:p.Arg1375=
ENST00000590574.5:c.4114C= ENSP00000466963.1:p.Arg1372=
ENST00000591595.5:n.2186C=
ENST00000592158.1:c.292C= ENSP00000467200.1:p.Arg98=
ENST00000592604.5:n.2036C=
NM_001128844.1:c.4213C= NP_001122316.1:p.Arg1405=
NM_001128845.1:c.4123C= NP_001122317.1:p.Arg1375=
NM_001128846.1:c.4123C= NP_001122318.1:p.Arg1375=
NM_001128847.1:c.4114C= NP_001122319.1:p.Arg1372=
NM_001128848.1:c.4114C= NP_001122320.1:p.Arg1372=
NM_001128849.1:c.4309C= NP_001122321.1:p.Arg1437=
NM_003072.3:c.4213C= NP_003063.2:p.Arg1405=
XM_005260028.2:c.4222C= XP_005260085.1:p.Arg1408=
XM_005260030.2:c.4210C= XP_005260087.1:p.Arg1404=
XM_005260031.2:c.4213C= XP_005260088.1:p.Arg1405=
XM_005260032.2:c.4123C= XP_005260089.1:p.Arg1375=
XM_005260033.2:c.4123C= XP_005260090.1:p.Arg1375=
XM_005260034.2:c.4114C= XP_005260091.1:p.Arg1372=
XM_005260035.2:c.4114C= XP_005260092.1:p.Arg1372=
XM_006722845.2:c.4309C= XP_006722908.1:p.Arg1437=
XM_006722846.2:c.4309C= XP_006722909.1:p.Arg1437=
XM_006722847.2:c.4309C= XP_006722910.1:p.Arg1437=
XM_011528198.1:c.4309C= XP_011526500.1:p.Arg1437=
XM_024451658.1:c.4309C= XP_024307426.1:p.Arg1437=
XM_024451659.1:c.4309C= XP_024307427.1:p.Arg1437=
XM_024451660.1:c.4222C= XP_024307428.1:p.Arg1408=
XM_024451661.1:c.4210C= XP_024307429.1:p.Arg1404=
XM_024451662.1:c.4213C= XP_024307430.1:p.Arg1405=
XM_024451663.1:c.4210C= XP_024307431.1:p.Arg1404=
XM_024451664.1:c.4123C= XP_024307432.1:p.Arg1375=
XM_024451665.1:c.4123C= XP_024307433.1:p.Arg1375=
XM_024451666.1:c.4114C= XP_024307434.1:p.Arg1372=
XM_024451667.1:c.4114C= XP_024307435.1:p.Arg1372=
NM_001128844.3:c.4213C= NP_001122316.1:p.Arg1405=
NM_001128845.2:c.4123C= NP_001122317.1:p.Arg1375=
NM_001128846.2:c.4123C= NP_001122318.1:p.Arg1375=
NM_001128847.4:c.4114C= NP_001122319.1:p.Arg1372=
NM_001128848.2:c.4114C= NP_001122320.1:p.Arg1372=
NM_001128849.3:c.4309C= NP_001122321.1:p.Arg1437=
NM_001374457.1:c.4114C= NP_001361386.1:p.Arg1372=
NM_003072.5:c.4213C= MANE Select NP_003063.2:p.Arg1405=
NR_164683.1:n.4603C=
NM_001387283.1:c.4309C= MANE Plus Clinical NP_001374212.1:p.Arg1437=