Canonical Allele Identifier: CA2579695734
Gene: SH2D1A HGNC NCBI
STAG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.124346570G>C , CM000685.2:g.124346570G>C GRCh38
NC_000023.10:g.123480420G>C , CM000685.1:g.123480420G>C GRCh37
NC_000023.9:g.123308101G>C NCBI36
NG_007464.1:g.5271G>C , LRG_106:g.5271G>C
NG_033796.2:g.391011G>C , LRG_782:g.391011G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360027.5:c.-73G>C (SH2D1A) ENSP00000353126.4:n.-73G>C
ENST00000647259.2:c.-73G>C (SH2D1A) ENSP00000494582.1:n.-73G>C
ENST00000698112.1:n.499-19191G>C (SH2D1A)
ENST00000698113.1:c.-73G>C (SH2D1A) ENSP00000513571.1:n.-73G>C
ENST00000698114.1:n.116+84G>C (SH2D1A)
ENST00000698115.1:n.72+84G>C (SH2D1A)
ENST00000698116.1:c.-58-15G>C (SH2D1A) ENSP00000513572.1:n.-58-15G>C
ENST00000698117.1:c.-73G>C (SH2D1A) ENSP00000513573.1:n.-73G>C
ENST00000371139.9:c.-73G>C (SH2D1A) MANE Select ENSP00000360181.5:n.-73G>C
ENST00000647259.1:c.-73G>C (SH2D1A) ENSP00000494582.1:n.-73G>C
ENST00000360027.4:c.-73G>C (SH2D1A) ENSP00000353126.4:n.-73G>C
ENST00000371139.8:c.-73G>C (SH2D1A) ENSP00000360181.4:n.-73G>C
ENST00000469481.1:n.454-65252G>C (STAG2)
ENST00000635645.1:n.499-19191G>C (SH2D1A)
NM_001114937.2:c.-73G>C (SH2D1A) NP_001108409.1:n.-73G>C
NM_002351.4:c.-73G>C , LRG_106t1:c.-73G>C (SH2D1A) NP_002342.1:n.-73G>C
NM_002351.5:c.-73G>C (SH2D1A) MANE Select NP_002342.1:n.-73G>C
NM_001114937.3:c.-73G>C (SH2D1A) NP_001108409.1:n.-73G>C