Canonical Allele Identifier: CA1827955829

Gene: SMARCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2123881C= , CM000671.2:g.2123881C=	GRCh38
NC_000009.11:g.2123881C= , CM000671.1:g.2123881C=	GRCh37
NC_000009.10:g.2113881C=	NCBI36
NG_032162.1:g.113540C=
NG_032162.2:g.148592C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000704350.1:c.3565C=	ENSP00000515861.1:p.Arg1189=
ENST00000704352.1:c.1174-37805C=	ENSP00000515863.1:n.1174-37805C=
ENST00000704353.1:c.1174-37805C=	ENSP00000515864.1:n.1174-37805C=
ENST00000704354.1:c.3909C=
ENST00000704355.1:c.2289C=
ENST00000349721.8:c.3925C= MANE Select	ENSP00000265773.5:p.Arg1309=
ENST00000357248.8:c.3925C=	ENSP00000349788.2:p.Arg1309=
ENST00000635739.1:n.2593C=
ENST00000636157.1:n.1532C=
ENST00000638139.1:n.959C=
ENST00000639760.2:c.32C=
ENST00000349721.7:c.3925C=	ENSP00000265773.5:p.Arg1309=
ENST00000357248.7:c.3925C=	ENSP00000349788.2:p.Arg1309=
ENST00000382194.6:c.3925C=	ENSP00000371629.1:p.Arg1309=
ENST00000382203.5:c.3925C=	ENSP00000371638.1:p.Arg1309=
ENST00000450198.6:c.3751C=	ENSP00000392081.2:p.Arg1251=
ENST00000634760.1:c.3925C=	ENSP00000489256.1:p.Arg1309=
ENST00000634772.1:c.302C=
ENST00000634925.1:n.1416C=
NM_001289396.1:c.3925C=	NP_001276325.1:p.Arg1309=
NM_001289397.1:c.3751C=	NP_001276326.1:p.Arg1251=
NM_003070.4:c.3925C=	NP_003061.3:p.Arg1309=
NM_139045.3:c.3925C=	NP_620614.2:p.Arg1309=
NM_003070.5:c.3925C= MANE Select	NP_003061.3:p.Arg1309=
NM_001289397.2:c.3751C=	NP_001276326.1:p.Arg1251=
NM_139045.4:c.3925C=	NP_620614.2:p.Arg1309=