Canonical Allele Identifier: CA518122587

Gene: SH2D1A STAG2

Linked Data

• MyVariant Identifiers: chrX:g.123480558C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.124346708C>G , CM000685.2:g.124346708C>G	GRCh38
NC_000023.10:g.123480558C>G , CM000685.1:g.123480558C>G	GRCh37
NC_000023.9:g.123308239C>G	NCBI36
NG_007464.1:g.5409C>G , LRG_106:g.5409C>G
NG_033796.2:g.391149C>G , LRG_782:g.391149C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360027.5:c.66C>G (SH2D1A)	ENSP00000353126.4:p.Ala22=
ENST00000647259.2:c.66C>G (SH2D1A)	ENSP00000494582.1:p.Ala22=
ENST00000698112.1:n.499-19053C>G (SH2D1A)
ENST00000698113.1:c.66C>G (SH2D1A)	ENSP00000513571.1:p.Ala22=
ENST00000698114.1:n.116+222C>G (SH2D1A)
ENST00000698115.1:n.72+222C>G (SH2D1A)
ENST00000698116.1:c.66C>G (SH2D1A)	ENSP00000513572.1:p.Ala22=
ENST00000698117.1:c.66C>G (SH2D1A)	ENSP00000513573.1:p.Ala22=
ENST00000698118.1:c.66C>G (SH2D1A)	ENSP00000513574.1:p.Ala22=
ENST00000371139.9:c.66C>G (SH2D1A) MANE Select	ENSP00000360181.5:p.Ala22=
ENST00000647259.1:c.66C>G (SH2D1A)	ENSP00000494582.1:p.Ala22=
ENST00000360027.4:c.66C>G (SH2D1A)	ENSP00000353126.4:p.Ala22=
ENST00000371139.8:c.66C>G (SH2D1A)	ENSP00000360181.4:p.Ala22=
ENST00000469481.1:n.454-65114C>G (STAG2)
ENST00000477673.2:c.66C>G (SH2D1A)	ENSP00000477094.1:p.Ala22=
ENST00000491950.5:n.120C>G (SH2D1A)
ENST00000494073.5:n.120C>G (SH2D1A)
ENST00000635645.1:n.499-19053C>G (SH2D1A)
NM_001114937.2:c.66C>G (SH2D1A)	NP_001108409.1:p.Ala22=
NM_002351.4:c.66C>G , LRG_106t1:c.66C>G (SH2D1A)	NP_002342.1:p.Ala22=
NM_002351.5:c.66C>G (SH2D1A) MANE Select	NP_002342.1:p.Ala22=
NM_001114937.3:c.66C>G (SH2D1A)	NP_001108409.1:p.Ala22=