Canonical Allele Identifier: CA2469659935
Gene: SRY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2786976T= , CM000686.2:g.2786976T= GRCh38
NC_000024.9:g.2655017T= , CM000686.1:g.2655017T= GRCh37
NC_000024.8:g.2715017T= NCBI36
NG_011751.1:g.5776A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000679518.1:n.106+12237T=
ENST00000679825.1:n.107-19T=
ENST00000680285.1:n.320-2773T=
ENST00000680845.1:n.107-19T=
ENST00000681787.1:n.106+12237T=
ENST00000681940.1:n.106+12237T=
ENST00000383070.2:c.*13A= MANE Select ENSP00000372547.1:n.*13A=
ENST00000383070.1:c.*13A= ENSP00000372547.1:n.*13A=
NM_003140.2:c.*13A= NP_003131.1:n.*13A=
NM_003140.3:c.*13A= MANE Select NP_003131.1:n.*13A=