Canonical Allele Identifier: CA414941930
Gene: SRY HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2787559A>T , CM000686.2:g.2787559A>T GRCh38
NC_000024.9:g.2655600A>T , CM000686.1:g.2655600A>T GRCh37
NC_000024.8:g.2715600A>T NCBI36
NG_011751.1:g.5193T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000679518.1:n.106+12820A>T
ENST00000679825.1:n.671A>T
ENST00000680285.1:n.320-2190A>T
ENST00000680845.1:n.245A>T
ENST00000681787.1:n.106+12820A>T
ENST00000681940.1:n.106+12820A>T
ENST00000383070.2:c.45T>A MANE Select ENSP00000372547.1:p.Asp15Glu
ENST00000383070.1:c.45T>A ENSP00000372547.1:p.Asp15Glu
NM_003140.2:c.45T>A NP_003131.1:p.Asp15Glu
NM_003140.3:c.45T>A MANE Select NP_003131.1:p.Asp15Glu