Canonical Allele Identifier: CA414941555
Gene: SRY HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2787398A>T , CM000686.2:g.2787398A>T GRCh38
NC_000024.9:g.2655439A>T , CM000686.1:g.2655439A>T GRCh37
NC_000024.8:g.2715439A>T NCBI36
NG_011751.1:g.5354T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000679518.1:n.106+12659A>T
ENST00000679825.1:n.510A>T
ENST00000680285.1:n.320-2351A>T
ENST00000680845.1:n.166-82A>T
ENST00000681787.1:n.106+12659A>T
ENST00000681940.1:n.106+12659A>T
ENST00000383070.2:c.206T>A MANE Select ENSP00000372547.1:p.Val69Glu
ENST00000383070.1:c.206T>A ENSP00000372547.1:p.Val69Glu
NM_003140.2:c.206T>A NP_003131.1:p.Val69Glu
NM_003140.3:c.206T>A MANE Select NP_003131.1:p.Val69Glu