Canonical Allele Identifier: CA414941827
Gene: SRY HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2787514T>A , CM000686.2:g.2787514T>A GRCh38
NC_000024.9:g.2655555T>A , CM000686.1:g.2655555T>A GRCh37
NC_000024.8:g.2715555T>A NCBI36
NG_011751.1:g.5238A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000679518.1:n.106+12775T>A
ENST00000679825.1:n.626T>A
ENST00000680285.1:n.320-2235T>A
ENST00000680845.1:n.200T>A
ENST00000681787.1:n.106+12775T>A
ENST00000681940.1:n.106+12775T>A
ENST00000383070.2:c.90A>T MANE Select ENSP00000372547.1:p.Arg30Ser
ENST00000383070.1:c.90A>T ENSP00000372547.1:p.Arg30Ser
NM_003140.2:c.90A>T NP_003131.1:p.Arg30Ser
NM_003140.3:c.90A>T MANE Select NP_003131.1:p.Arg30Ser