Canonical Allele Identifier: CA414122346

Gene: SH2D1A STAG2

Linked Data

• MyVariant Identifiers: chrX:g.123480578A>C (hg19) ; chrX:g.124346728A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.124346728A>C , CM000685.2:g.124346728A>C	GRCh38
NC_000023.10:g.123480578A>C , CM000685.1:g.123480578A>C	GRCh37
NC_000023.9:g.123308259A>C	NCBI36
NG_007464.1:g.5429A>C , LRG_106:g.5429A>C
NG_033796.2:g.391169A>C , LRG_782:g.391169A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360027.5:c.86A>C (SH2D1A)	ENSP00000353126.4:p.Tyr29Ser
ENST00000647259.2:c.86A>C (SH2D1A)	ENSP00000494582.1:p.Tyr29Ser
ENST00000698112.1:n.499-19033A>C (SH2D1A)
ENST00000698113.1:c.86A>C (SH2D1A)	ENSP00000513571.1:p.Tyr29Ser
ENST00000698114.1:n.116+242A>C (SH2D1A)
ENST00000698115.1:n.72+242A>C (SH2D1A)
ENST00000698116.1:c.86A>C (SH2D1A)	ENSP00000513572.1:p.Tyr29Ser
ENST00000698117.1:c.86A>C (SH2D1A)	ENSP00000513573.1:p.Tyr29Ser
ENST00000698118.1:c.86A>C (SH2D1A)	ENSP00000513574.1:p.Tyr29Ser
ENST00000371139.9:c.86A>C (SH2D1A) MANE Select	ENSP00000360181.5:p.Tyr29Ser
ENST00000647259.1:c.86A>C (SH2D1A)	ENSP00000494582.1:p.Tyr29Ser
ENST00000360027.4:c.86A>C (SH2D1A)	ENSP00000353126.4:p.Tyr29Ser
ENST00000371139.8:c.86A>C (SH2D1A)	ENSP00000360181.4:p.Tyr29Ser
ENST00000469481.1:n.454-65094A>C (STAG2)
ENST00000477673.2:c.86A>C (SH2D1A)	ENSP00000477094.1:p.Tyr29Ser
ENST00000491950.5:n.140A>C (SH2D1A)
ENST00000494073.5:n.140A>C (SH2D1A)
ENST00000635645.1:n.499-19033A>C (SH2D1A)
NM_001114937.2:c.86A>C (SH2D1A)	NP_001108409.1:p.Tyr29Ser
NM_002351.4:c.86A>C , LRG_106t1:c.86A>C (SH2D1A)	NP_002342.1:p.Tyr29Ser
NM_002351.5:c.86A>C (SH2D1A) MANE Select	NP_002342.1:p.Tyr29Ser
NM_001114937.3:c.86A>C (SH2D1A)	NP_001108409.1:p.Tyr29Ser