Canonical Allele Identifier: CA414940736
Gene: SRY HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2787047A>T , CM000686.2:g.2787047A>T GRCh38
NC_000024.9:g.2655088A>T , CM000686.1:g.2655088A>T GRCh37
NC_000024.8:g.2715088A>T NCBI36
NG_011751.1:g.5705T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000679518.1:n.106+12308A>T
ENST00000679825.1:n.159A>T
ENST00000680285.1:n.320-2702A>T
ENST00000680845.1:n.159A>T
ENST00000681787.1:n.106+12308A>T
ENST00000681940.1:n.106+12308A>T
ENST00000383070.2:c.557T>A MANE Select ENSP00000372547.1:p.Ile186Asn
ENST00000383070.1:c.557T>A ENSP00000372547.1:p.Ile186Asn
NM_003140.2:c.557T>A NP_003131.1:p.Ile186Asn
NM_003140.3:c.557T>A MANE Select NP_003131.1:p.Ile186Asn