Canonical Allele Identifier: CA414124554
Community Standard Title: NM_002351.5(SH2D1A):c.251T>C (p.Ile84Thr)
Gene: SH2D1A HGNC NCBI
STAG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.124370225T>C , CM000685.2:g.124370225T>C GRCh38
NC_000023.10:g.123504075T>C , CM000685.1:g.123504075T>C GRCh37
NC_000023.9:g.123331756T>C NCBI36
NG_007464.1:g.28926T>C , LRG_106:g.28926T>C
NG_033796.2:g.414666T>C , LRG_782:g.414666T>C

Transcript Alleles

HGVS Amino-acid Change
NM_002351.5:c.251T>C (SH2D1A) MANE Select NP_002342.1:p.Ile84Thr
ENST00000371139.9:c.251T>C (SH2D1A) MANE Select ENSP00000360181.5:p.Ile84Thr
NM_001114937.2:c.251T>C (SH2D1A) NP_001108409.1:p.Ile84Thr
NM_001114937.3:c.251T>C (SH2D1A) NP_001108409.1:p.Ile84Thr
NM_002351.4:c.251T>C , LRG_106t1:c.251T>C (SH2D1A) NP_002342.1:p.Ile84Thr
ENST00000360027.4:c.251T>C (SH2D1A) ENSP00000353126.4:p.Ile84Thr
ENST00000360027.5:c.251T>C (SH2D1A) ENSP00000353126.4:p.Ile84Thr
ENST00000371139.8:c.251T>C (SH2D1A) ENSP00000360181.4:p.Ile84Thr
ENST00000469481.1:n.454-41597T>C (STAG2)
ENST00000477673.2:c.180-6T>C (SH2D1A) ENSP00000477094.1:n.180-6T>C
ENST00000491950.5:n.241T>C (SH2D1A)
ENST00000494073.5:n.192-6T>C (SH2D1A)
ENST00000635645.1:n.612T>C (SH2D1A)
ENST00000647259.1:c.*89T>C (SH2D1A) ENSP00000494582.1:n.*89T>C
ENST00000647259.2:c.*89T>C (SH2D1A) ENSP00000494582.1:n.*89T>C
ENST00000698112.1:n.563-6T>C (SH2D1A)
ENST00000698113.1:c.251T>C (SH2D1A) ENSP00000513571.1:p.Ile84Thr
ENST00000698114.1:n.117-6T>C (SH2D1A)
ENST00000698115.1:n.186T>C (SH2D1A)
ENST00000698116.1:c.251T>C (SH2D1A) ENSP00000513572.1:p.Ile84Thr
ENST00000698117.1:c.202-6T>C (SH2D1A) ENSP00000513573.1:n.202-6T>C
ENST00000698118.1:c.251T>C (SH2D1A) ENSP00000513574.1:p.Ile84Thr
ENST00000698119.1:n.550T>C (SH2D1A)
ENST00000698120.1:n.94-6T>C (SH2D1A)