Canonical Allele Identifier: CA2694635530
Gene: SH2D1A HGNC NCBI
STAG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.124346580A>T , CM000685.2:g.124346580A>T GRCh38
NC_000023.10:g.123480430A>T , CM000685.1:g.123480430A>T GRCh37
NC_000023.9:g.123308111A>T NCBI36
NG_007464.1:g.5281A>T , LRG_106:g.5281A>T
NG_033796.2:g.391021A>T , LRG_782:g.391021A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360027.5:c.-63A>T (SH2D1A) ENSP00000353126.4:n.-63A>T
ENST00000647259.2:c.-63A>T (SH2D1A) ENSP00000494582.1:n.-63A>T
ENST00000698112.1:n.499-19181A>T (SH2D1A)
ENST00000698113.1:c.-63A>T (SH2D1A) ENSP00000513571.1:n.-63A>T
ENST00000698114.1:n.116+94A>T (SH2D1A)
ENST00000698115.1:n.72+94A>T (SH2D1A)
ENST00000698116.1:c.-58-5A>T (SH2D1A) ENSP00000513572.1:n.-58-5A>T
ENST00000698117.1:c.-63A>T (SH2D1A) ENSP00000513573.1:n.-63A>T
ENST00000371139.9:c.-63A>T (SH2D1A) MANE Select ENSP00000360181.5:n.-63A>T
ENST00000647259.1:c.-63A>T (SH2D1A) ENSP00000494582.1:n.-63A>T
ENST00000360027.4:c.-63A>T (SH2D1A) ENSP00000353126.4:n.-63A>T
ENST00000371139.8:c.-63A>T (SH2D1A) ENSP00000360181.4:n.-63A>T
ENST00000469481.1:n.454-65242A>T (STAG2)
ENST00000635645.1:n.499-19181A>T (SH2D1A)
NM_001114937.2:c.-63A>T (SH2D1A) NP_001108409.1:n.-63A>T
NM_002351.4:c.-63A>T , LRG_106t1:c.-63A>T (SH2D1A) NP_002342.1:n.-63A>T
NM_002351.5:c.-63A>T (SH2D1A) MANE Select NP_002342.1:n.-63A>T
NM_001114937.3:c.-63A>T (SH2D1A) NP_001108409.1:n.-63A>T