Canonical Allele Identifier: CA414122374

Gene: SH2D1A STAG2

Linked Data

• ClinVar Variation Id: 871638
• ClinVar RCV Id: RCV001091712
• dbSNP Id: rs2059993731
• MyVariant Identifiers: chrX:g.123480590A>G (hg19) ; chrX:g.124346740A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.124346740A>G , CM000685.2:g.124346740A>G	GRCh38
NC_000023.10:g.123480590A>G , CM000685.1:g.123480590A>G	GRCh37
NC_000023.9:g.123308271A>G	NCBI36
NG_007464.1:g.5441A>G , LRG_106:g.5441A>G
NG_033796.2:g.391181A>G , LRG_782:g.391181A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360027.5:c.98A>G (SH2D1A)	ENSP00000353126.4:p.Asp33Gly
ENST00000647259.2:c.98A>G (SH2D1A)	ENSP00000494582.1:p.Asp33Gly
ENST00000698112.1:n.499-19021A>G (SH2D1A)
ENST00000698113.1:c.98A>G (SH2D1A)	ENSP00000513571.1:p.Asp33Gly
ENST00000698114.1:n.116+254A>G (SH2D1A)
ENST00000698115.1:n.72+254A>G (SH2D1A)
ENST00000698116.1:c.98A>G (SH2D1A)	ENSP00000513572.1:p.Asp33Gly
ENST00000698117.1:c.98A>G (SH2D1A)	ENSP00000513573.1:p.Asp33Gly
ENST00000698118.1:c.98A>G (SH2D1A)	ENSP00000513574.1:p.Asp33Gly
ENST00000371139.9:c.98A>G (SH2D1A) MANE Select	ENSP00000360181.5:p.Asp33Gly
ENST00000647259.1:c.98A>G (SH2D1A)	ENSP00000494582.1:p.Asp33Gly
ENST00000360027.4:c.98A>G (SH2D1A)	ENSP00000353126.4:p.Asp33Gly
ENST00000371139.8:c.98A>G (SH2D1A)	ENSP00000360181.4:p.Asp33Gly
ENST00000469481.1:n.454-65082A>G (STAG2)
ENST00000477673.2:c.98A>G (SH2D1A)	ENSP00000477094.1:p.Asp33Gly
ENST00000491950.5:n.152A>G (SH2D1A)
ENST00000494073.5:n.152A>G (SH2D1A)
ENST00000635645.1:n.499-19021A>G (SH2D1A)
NM_001114937.2:c.98A>G (SH2D1A)	NP_001108409.1:p.Asp33Gly
NM_002351.4:c.98A>G , LRG_106t1:c.98A>G (SH2D1A)	NP_002342.1:p.Asp33Gly
NM_002351.5:c.98A>G (SH2D1A) MANE Select	NP_002342.1:p.Asp33Gly
NM_001114937.3:c.98A>G (SH2D1A)	NP_001108409.1:p.Asp33Gly