Canonical Allele Identifier: CA2469659936
Gene: SRY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2786984T= , CM000686.2:g.2786984T= GRCh38
NC_000024.9:g.2655025T= , CM000686.1:g.2655025T= GRCh37
NC_000024.8:g.2715025T= NCBI36
NG_011751.1:g.5768A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000679518.1:n.106+12245T=
ENST00000679825.1:n.107-11T=
ENST00000680285.1:n.320-2765T=
ENST00000680845.1:n.107-11T=
ENST00000681787.1:n.106+12245T=
ENST00000681940.1:n.106+12245T=
ENST00000383070.2:c.*5A= MANE Select ENSP00000372547.1:n.*5A=
ENST00000383070.1:c.*5A= ENSP00000372547.1:n.*5A=
NM_003140.2:c.*5A= NP_003131.1:n.*5A=
NM_003140.3:c.*5A= MANE Select NP_003131.1:n.*5A=