Canonical Allele Identifier: CA414122346
Gene: SH2D1A HGNC NCBI
STAG2 HGNC NCBI

Linked Data

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