Canonical Allele Identifier: CA2694636330

Gene: SH2D1A STAG2

Linked Data

• gnomAD v4: X-124370081-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.124370081A>C , CM000685.2:g.124370081A>C	GRCh38
NC_000023.10:g.123503931A>C , CM000685.1:g.123503931A>C	GRCh37
NC_000023.9:g.123331612A>C	NCBI36
NG_007464.1:g.28782A>C , LRG_106:g.28782A>C
NG_033796.2:g.414522A>C , LRG_782:g.414522A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360027.5:c.202-95A>C (SH2D1A)	ENSP00000353126.4:n.202-95A>C
ENST00000647259.2:c.*40-95A>C (SH2D1A)	ENSP00000494582.1:n.*40-95A>C
ENST00000698112.1:n.563-150A>C (SH2D1A)
ENST00000698113.1:c.202-95A>C (SH2D1A)	ENSP00000513571.1:n.202-95A>C
ENST00000698114.1:n.117-150A>C (SH2D1A)
ENST00000698115.1:n.137-95A>C (SH2D1A)
ENST00000698116.1:c.202-95A>C (SH2D1A)	ENSP00000513572.1:n.202-95A>C
ENST00000698117.1:c.202-150A>C (SH2D1A)	ENSP00000513573.1:n.202-150A>C
ENST00000698118.1:c.202-95A>C (SH2D1A)	ENSP00000513574.1:n.202-95A>C
ENST00000698119.1:n.501-95A>C (SH2D1A)
ENST00000698120.1:n.31A>C (SH2D1A)
ENST00000371139.9:c.202-95A>C (SH2D1A) MANE Select	ENSP00000360181.5:n.202-95A>C
ENST00000647259.1:c.*40-95A>C (SH2D1A)	ENSP00000494582.1:n.*40-95A>C
ENST00000360027.4:c.202-95A>C (SH2D1A)	ENSP00000353126.4:n.202-95A>C
ENST00000371139.8:c.202-95A>C (SH2D1A)	ENSP00000360181.4:n.202-95A>C
ENST00000469481.1:n.454-41741A>C (STAG2)
ENST00000477673.2:c.180-150A>C (SH2D1A)	ENSP00000477094.1:n.180-150A>C
ENST00000491950.5:n.192-95A>C (SH2D1A)
ENST00000494073.5:n.192-150A>C (SH2D1A)
ENST00000635645.1:n.563-95A>C (SH2D1A)
NM_001114937.2:c.202-95A>C (SH2D1A)	NP_001108409.1:n.202-95A>C
NM_002351.4:c.202-95A>C , LRG_106t1:c.202-95A>C (SH2D1A)	NP_002342.1:n.202-95A>C
NM_002351.5:c.202-95A>C (SH2D1A) MANE Select	NP_002342.1:n.202-95A>C
NM_001114937.3:c.202-95A>C (SH2D1A)	NP_001108409.1:n.202-95A>C