Canonical Allele Identifier: CA1827948992

Gene: SMARCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2110274C= , CM000671.2:g.2110274C=	GRCh38
NC_000009.11:g.2110274C= , CM000671.1:g.2110274C=	GRCh37
NC_000009.10:g.2100274C=	NCBI36
NG_032162.1:g.99933C=
NG_032162.2:g.134985C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000637134.2:c.3313C=	ENSP00000489667.2:p.Arg1105=
ENST00000704350.1:c.2953C=	ENSP00000515861.1:p.Arg985=
ENST00000704352.1:c.1174-51412C=	ENSP00000515863.1:n.1174-51412C=
ENST00000704353.1:c.1174-51412C=	ENSP00000515864.1:n.1174-51412C=
ENST00000704354.1:c.3297C=
ENST00000704355.1:c.1677C=
ENST00000349721.8:c.3313C= MANE Select	ENSP00000265773.5:p.Arg1105=
ENST00000357248.8:c.3313C=	ENSP00000349788.2:p.Arg1105=
ENST00000635739.1:n.1981C=
ENST00000636157.1:n.920C=
ENST00000638139.1:n.347C=
ENST00000349721.7:c.3313C=	ENSP00000265773.5:p.Arg1105=
ENST00000357248.7:c.3313C=	ENSP00000349788.2:p.Arg1105=
ENST00000382194.6:c.3313C=	ENSP00000371629.1:p.Arg1105=
ENST00000382203.5:c.3313C=	ENSP00000371638.1:p.Arg1105=
ENST00000450198.6:c.3139C=	ENSP00000392081.2:p.Arg1047=
ENST00000634271.1:n.486C=
ENST00000634760.1:c.3313C=	ENSP00000489256.1:p.Arg1105=
ENST00000634925.1:n.804C=
NM_001289396.1:c.3313C=	NP_001276325.1:p.Arg1105=
NM_001289397.1:c.3139C=	NP_001276326.1:p.Arg1047=
NM_003070.4:c.3313C=	NP_003061.3:p.Arg1105=
NM_139045.3:c.3313C=	NP_620614.2:p.Arg1105=
NM_003070.5:c.3313C= MANE Select	NP_003061.3:p.Arg1105=
NM_001289397.2:c.3139C=	NP_001276326.1:p.Arg1047=
NM_139045.4:c.3313C=	NP_620614.2:p.Arg1105=