Canonical Allele Identifier: CA518122133

Gene: SH2D1A STAG2

Linked Data

• dbSNP Id: rs1298636213
• gnomAD v2: X-123480498-C-T
• gnomAD v4: X-124346648-C-T
• COSMIC: COSM1625473
• MyVariant Identifiers: chrX:g.123480498C>T (hg19) ; chrX:g.124346648C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.124346648C>T , CM000685.2:g.124346648C>T	GRCh38
NC_000023.10:g.123480498C>T , CM000685.1:g.123480498C>T	GRCh37
NC_000023.9:g.123308179C>T	NCBI36
NG_007464.1:g.5349C>T , LRG_106:g.5349C>T
NG_033796.2:g.391089C>T , LRG_782:g.391089C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360027.5:c.6C>T (SH2D1A)	ENSP00000353126.4:p.Asp2=
ENST00000647259.2:c.6C>T (SH2D1A)	ENSP00000494582.1:p.Asp2=
ENST00000698112.1:n.499-19113C>T (SH2D1A)
ENST00000698113.1:c.6C>T (SH2D1A)	ENSP00000513571.1:p.Asp2=
ENST00000698114.1:n.116+162C>T (SH2D1A)
ENST00000698115.1:n.72+162C>T (SH2D1A)
ENST00000698116.1:c.6C>T (SH2D1A)	ENSP00000513572.1:p.Asp2=
ENST00000698117.1:c.6C>T (SH2D1A)	ENSP00000513573.1:p.Asp2=
ENST00000698118.1:c.6C>T (SH2D1A)	ENSP00000513574.1:p.Asp2=
ENST00000371139.9:c.6C>T (SH2D1A) MANE Select	ENSP00000360181.5:p.Asp2=
ENST00000647259.1:c.6C>T (SH2D1A)	ENSP00000494582.1:p.Asp2=
ENST00000360027.4:c.6C>T (SH2D1A)	ENSP00000353126.4:p.Asp2=
ENST00000371139.8:c.6C>T (SH2D1A)	ENSP00000360181.4:p.Asp2=
ENST00000469481.1:n.454-65174C>T (STAG2)
ENST00000477673.2:c.6C>T (SH2D1A)	ENSP00000477094.1:p.Asp2=
ENST00000491950.5:n.60C>T (SH2D1A)
ENST00000494073.5:n.60C>T (SH2D1A)
ENST00000635645.1:n.499-19113C>T (SH2D1A)
NM_001114937.2:c.6C>T (SH2D1A)	NP_001108409.1:p.Asp2=
NM_002351.4:c.6C>T , LRG_106t1:c.6C>T (SH2D1A)	NP_002342.1:p.Asp2=
NM_002351.5:c.6C>T (SH2D1A) MANE Select	NP_002342.1:p.Asp2=
NM_001114937.3:c.6C>T (SH2D1A)	NP_001108409.1:p.Asp2=