Canonical Allele Identifier: CA414941318
Gene: SRY HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2787296T>A , CM000686.2:g.2787296T>A GRCh38
NC_000024.9:g.2655337T>A , CM000686.1:g.2655337T>A GRCh37
NC_000024.8:g.2715337T>A NCBI36
NG_011751.1:g.5456A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000679518.1:n.106+12557T>A
ENST00000679825.1:n.408T>A
ENST00000680285.1:n.320-2453T>A
ENST00000680845.1:n.166-184T>A
ENST00000681787.1:n.106+12557T>A
ENST00000681940.1:n.106+12557T>A
ENST00000383070.2:c.308A>T MANE Select ENSP00000372547.1:p.Glu103Val
ENST00000383070.1:c.308A>T ENSP00000372547.1:p.Glu103Val
NM_003140.2:c.308A>T NP_003131.1:p.Glu103Val
NM_003140.3:c.308A>T MANE Select NP_003131.1:p.Glu103Val