Canonical Allele Identifier: CA1827951792

Gene: SMARCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2115902C= , CM000671.2:g.2115902C=	GRCh38
NC_000009.11:g.2115902C= , CM000671.1:g.2115902C=	GRCh37
NC_000009.10:g.2105902C=	NCBI36
NG_032162.1:g.105561C=
NG_032162.2:g.140613C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704350.1:c.3177C=	ENSP00000515861.1:p.Ser1059=
ENST00000704352.1:c.1174-45784C=	ENSP00000515863.1:n.1174-45784C=
ENST00000704353.1:c.1174-45784C=	ENSP00000515864.1:n.1174-45784C=
ENST00000704354.1:c.3521C=
ENST00000704355.1:c.1901C=
ENST00000349721.8:c.3537C= MANE Select	ENSP00000265773.5:p.Ser1179=
ENST00000357248.8:c.3537C=	ENSP00000349788.2:p.Ser1179=
ENST00000635739.1:n.2205C=
ENST00000636157.1:n.1144C=
ENST00000638139.1:n.571C=
ENST00000349721.7:c.3537C=	ENSP00000265773.5:p.Ser1179=
ENST00000357248.7:c.3537C=	ENSP00000349788.2:p.Ser1179=
ENST00000382194.6:c.3537C=	ENSP00000371629.1:p.Ser1179=
ENST00000382203.5:c.3537C=	ENSP00000371638.1:p.Ser1179=
ENST00000450198.6:c.3363C=	ENSP00000392081.2:p.Ser1121=
ENST00000634760.1:c.3537C=	ENSP00000489256.1:p.Ser1179=
ENST00000634772.1:c.62-3556C=
ENST00000634925.1:n.1028C=
NM_001289396.1:c.3537C=	NP_001276325.1:p.Ser1179=
NM_001289397.1:c.3363C=	NP_001276326.1:p.Ser1121=
NM_003070.4:c.3537C=	NP_003061.3:p.Ser1179=
NM_139045.3:c.3537C=	NP_620614.2:p.Ser1179=
NM_003070.5:c.3537C= MANE Select	NP_003061.3:p.Ser1179=
NM_001289397.2:c.3363C=	NP_001276326.1:p.Ser1121=
NM_139045.4:c.3537C=	NP_620614.2:p.Ser1179=