Canonical Allele Identifier: CA1827951778

Gene: SMARCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2115858C= , CM000671.2:g.2115858C=	GRCh38
NC_000009.11:g.2115858C= , CM000671.1:g.2115858C=	GRCh37
NC_000009.10:g.2105858C=	NCBI36
NG_032162.1:g.105517C=
NG_032162.2:g.140569C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704350.1:c.3133C=	ENSP00000515861.1:p.Gln1045=
ENST00000704352.1:c.1174-45828C=	ENSP00000515863.1:n.1174-45828C=
ENST00000704353.1:c.1174-45828C=	ENSP00000515864.1:n.1174-45828C=
ENST00000704354.1:c.3477C=
ENST00000704355.1:c.1857C=
ENST00000349721.8:c.3493C= MANE Select	ENSP00000265773.5:p.Gln1165=
ENST00000357248.8:c.3493C=	ENSP00000349788.2:p.Gln1165=
ENST00000635739.1:n.2161C=
ENST00000636157.1:n.1100C=
ENST00000638139.1:n.527C=
ENST00000349721.7:c.3493C=	ENSP00000265773.5:p.Gln1165=
ENST00000357248.7:c.3493C=	ENSP00000349788.2:p.Gln1165=
ENST00000382194.6:c.3493C=	ENSP00000371629.1:p.Gln1165=
ENST00000382203.5:c.3493C=	ENSP00000371638.1:p.Gln1165=
ENST00000450198.6:c.3319C=	ENSP00000392081.2:p.Gln1107=
ENST00000634760.1:c.3493C=	ENSP00000489256.1:p.Gln1165=
ENST00000634772.1:c.62-3600C=
ENST00000634925.1:n.984C=
NM_001289396.1:c.3493C=	NP_001276325.1:p.Gln1165=
NM_001289397.1:c.3319C=	NP_001276326.1:p.Gln1107=
NM_003070.4:c.3493C=	NP_003061.3:p.Gln1165=
NM_139045.3:c.3493C=	NP_620614.2:p.Gln1165=
NM_003070.5:c.3493C= MANE Select	NP_003061.3:p.Gln1165=
NM_001289397.2:c.3319C=	NP_001276326.1:p.Gln1107=
NM_139045.4:c.3493C=	NP_620614.2:p.Gln1165=