Canonical Allele Identifier: CA2469659934
Gene: SRY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2786973A= , CM000686.2:g.2786973A= GRCh38
NC_000024.9:g.2655014A= , CM000686.1:g.2655014A= GRCh37
NC_000024.8:g.2715014A= NCBI36
NG_011751.1:g.5779T=

Transcript Alleles

HGVS Amino-acid change
ENST00000679518.1:n.106+12234A=
ENST00000679825.1:n.107-22A=
ENST00000680285.1:n.320-2776A=
ENST00000680845.1:n.107-22A=
ENST00000681787.1:n.106+12234A=
ENST00000681940.1:n.106+12234A=
ENST00000383070.2:c.*16T= MANE Select ENSP00000372547.1:n.*16T=
ENST00000383070.1:c.*16T= ENSP00000372547.1:n.*16T=
NM_003140.2:c.*16T= NP_003131.1:n.*16T=
NM_003140.3:c.*16T= MANE Select NP_003131.1:n.*16T=