Canonical Allele Identifier: CA2456206958

Gene: SH2D1A STAG2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.124346456T= , CM000685.2:g.124346456T=	GRCh38
NC_000023.10:g.123480306T= , CM000685.1:g.123480306T=	GRCh37
NC_000023.9:g.123307987T=	NCBI36
NG_007464.1:g.5157T= , LRG_106:g.5157T=
NG_033796.2:g.390897T= , LRG_782:g.390897T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360027.5:c.-187T= (SH2D1A)	ENSP00000353126.4:n.-187T=
ENST00000647259.2:c.-187T= (SH2D1A)	ENSP00000494582.1:n.-187T=
ENST00000698112.1:n.499-19305T= (SH2D1A)
ENST00000698113.1:c.-187T= (SH2D1A)	ENSP00000513571.1:n.-187T=
ENST00000698114.1:n.86T= (SH2D1A)
ENST00000698115.1:n.42T= (SH2D1A)
ENST00000698116.1:c.-89T= (SH2D1A)	ENSP00000513572.1:n.-89T=
ENST00000647259.1:c.-187T= (SH2D1A)	ENSP00000494582.1:n.-187T=
ENST00000371139.8:c.-187T= (SH2D1A)	ENSP00000360181.4:n.-187T=
ENST00000469481.1:n.454-65366T= (STAG2)
ENST00000635645.1:n.499-19305T= (SH2D1A)
NM_001114937.2:c.-187T= (SH2D1A)	NP_001108409.1:n.-187T=
NM_002351.4:c.-187T= , LRG_106t1:c.-187T= (SH2D1A)	NP_002342.1:n.-187T=