Canonical Allele Identifier: CA1827951807

Gene: SMARCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2115952A= , CM000671.2:g.2115952A=	GRCh38
NC_000009.11:g.2115952A= , CM000671.1:g.2115952A=	GRCh37
NC_000009.10:g.2105952A=	NCBI36
NG_032162.1:g.105611A=
NG_032162.2:g.140663A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704350.1:c.3227A=	ENSP00000515861.1:p.Gln1076=
ENST00000704352.1:c.1174-45734A=	ENSP00000515863.1:n.1174-45734A=
ENST00000704353.1:c.1174-45734A=	ENSP00000515864.1:n.1174-45734A=
ENST00000704354.1:c.3571A=
ENST00000704355.1:c.1951A=
ENST00000349721.8:c.3587A= MANE Select	ENSP00000265773.5:p.Gln1196=
ENST00000357248.8:c.3587A=	ENSP00000349788.2:p.Gln1196=
ENST00000635739.1:n.2255A=
ENST00000636157.1:n.1194A=
ENST00000638139.1:n.621A=
ENST00000349721.7:c.3587A=	ENSP00000265773.5:p.Gln1196=
ENST00000357248.7:c.3587A=	ENSP00000349788.2:p.Gln1196=
ENST00000382194.6:c.3587A=	ENSP00000371629.1:p.Gln1196=
ENST00000382203.5:c.3587A=	ENSP00000371638.1:p.Gln1196=
ENST00000450198.6:c.3413A=	ENSP00000392081.2:p.Gln1138=
ENST00000634760.1:c.3587A=	ENSP00000489256.1:p.Gln1196=
ENST00000634772.1:c.62-3506A=
ENST00000634925.1:n.1078A=
NM_001289396.1:c.3587A=	NP_001276325.1:p.Gln1196=
NM_001289397.1:c.3413A=	NP_001276326.1:p.Gln1138=
NM_003070.4:c.3587A=	NP_003061.3:p.Gln1196=
NM_139045.3:c.3587A=	NP_620614.2:p.Gln1196=
NM_003070.5:c.3587A= MANE Select	NP_003061.3:p.Gln1196=
NM_001289397.2:c.3413A=	NP_001276326.1:p.Gln1138=
NM_139045.4:c.3587A=	NP_620614.2:p.Gln1196=