Canonical Allele Identifier: CA2469659940
Gene: SRY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2787044T= , CM000686.2:g.2787044T= GRCh38
NC_000024.9:g.2655085T= , CM000686.1:g.2655085T= GRCh37
NC_000024.8:g.2715085T= NCBI36
NG_011751.1:g.5708A=

Transcript Alleles

HGVS Amino-acid change
ENST00000679518.1:n.106+12305T=
ENST00000679825.1:n.156T=
ENST00000680285.1:n.320-2705T=
ENST00000680845.1:n.156T=
ENST00000681787.1:n.106+12305T=
ENST00000681940.1:n.106+12305T=
ENST00000383070.2:c.560A= MANE Select ENSP00000372547.1:p.Asn187=
ENST00000383070.1:c.560A= ENSP00000372547.1:p.Asn187=
NM_003140.2:c.560A= NP_003131.1:p.Asn187=
NM_003140.3:c.560A= MANE Select NP_003131.1:p.Asn187=