Canonical Allele Identifier: CA2694635488
Gene: SH2D1A HGNC NCBI
STAG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.124346498A>G , CM000685.2:g.124346498A>G GRCh38
NC_000023.10:g.123480348A>G , CM000685.1:g.123480348A>G GRCh37
NC_000023.9:g.123308029A>G NCBI36
NG_007464.1:g.5199A>G , LRG_106:g.5199A>G
NG_033796.2:g.390939A>G , LRG_782:g.390939A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360027.5:c.-145A>G (SH2D1A) ENSP00000353126.4:n.-145A>G
ENST00000647259.2:c.-145A>G (SH2D1A) ENSP00000494582.1:n.-145A>G
ENST00000698112.1:n.499-19263A>G (SH2D1A)
ENST00000698113.1:c.-145A>G (SH2D1A) ENSP00000513571.1:n.-145A>G
ENST00000698114.1:n.116+12A>G (SH2D1A)
ENST00000698115.1:n.72+12A>G (SH2D1A)
ENST00000698116.1:c.-59+12A>G (SH2D1A) ENSP00000513572.1:n.-59+12A>G
ENST00000647259.1:c.-145A>G (SH2D1A) ENSP00000494582.1:n.-145A>G
ENST00000371139.8:c.-145A>G (SH2D1A) ENSP00000360181.4:n.-145A>G
ENST00000469481.1:n.454-65324A>G (STAG2)
ENST00000635645.1:n.499-19263A>G (SH2D1A)
NM_001114937.2:c.-145A>G (SH2D1A) NP_001108409.1:n.-145A>G
NM_002351.4:c.-145A>G , LRG_106t1:c.-145A>G (SH2D1A) NP_002342.1:n.-145A>G