Canonical Allele Identifier: CA414122326

Gene: SH2D1A STAG2

Linked Data

• MyVariant Identifiers: chrX:g.123480569A>T (hg19) ; chrX:g.124346719A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.124346719A>T , CM000685.2:g.124346719A>T	GRCh38
NC_000023.10:g.123480569A>T , CM000685.1:g.123480569A>T	GRCh37
NC_000023.9:g.123308250A>T	NCBI36
NG_007464.1:g.5420A>T , LRG_106:g.5420A>T
NG_033796.2:g.391160A>T , LRG_782:g.391160A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360027.5:c.77A>T (SH2D1A)	ENSP00000353126.4:p.Asp26Val
ENST00000647259.2:c.77A>T (SH2D1A)	ENSP00000494582.1:p.Asp26Val
ENST00000698112.1:n.499-19042A>T (SH2D1A)
ENST00000698113.1:c.77A>T (SH2D1A)	ENSP00000513571.1:p.Asp26Val
ENST00000698114.1:n.116+233A>T (SH2D1A)
ENST00000698115.1:n.72+233A>T (SH2D1A)
ENST00000698116.1:c.77A>T (SH2D1A)	ENSP00000513572.1:p.Asp26Val
ENST00000698117.1:c.77A>T (SH2D1A)	ENSP00000513573.1:p.Asp26Val
ENST00000698118.1:c.77A>T (SH2D1A)	ENSP00000513574.1:p.Asp26Val
ENST00000371139.9:c.77A>T (SH2D1A) MANE Select	ENSP00000360181.5:p.Asp26Val
ENST00000647259.1:c.77A>T (SH2D1A)	ENSP00000494582.1:p.Asp26Val
ENST00000360027.4:c.77A>T (SH2D1A)	ENSP00000353126.4:p.Asp26Val
ENST00000371139.8:c.77A>T (SH2D1A)	ENSP00000360181.4:p.Asp26Val
ENST00000469481.1:n.454-65103A>T (STAG2)
ENST00000477673.2:c.77A>T (SH2D1A)	ENSP00000477094.1:p.Asp26Val
ENST00000491950.5:n.131A>T (SH2D1A)
ENST00000494073.5:n.131A>T (SH2D1A)
ENST00000635645.1:n.499-19042A>T (SH2D1A)
NM_001114937.2:c.77A>T (SH2D1A)	NP_001108409.1:p.Asp26Val
NM_002351.4:c.77A>T , LRG_106t1:c.77A>T (SH2D1A)	NP_002342.1:p.Asp26Val
NM_002351.5:c.77A>T (SH2D1A) MANE Select	NP_002342.1:p.Asp26Val
NM_001114937.3:c.77A>T (SH2D1A)	NP_001108409.1:p.Asp26Val