Canonical Allele Identifier: CA2469659931
Gene: SRY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2786965T= , CM000686.2:g.2786965T= GRCh38
NC_000024.9:g.2655006T= , CM000686.1:g.2655006T= GRCh37
NC_000024.8:g.2715006T= NCBI36
NG_011751.1:g.5787A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000679518.1:n.106+12226T=
ENST00000679825.1:n.107-30T=
ENST00000680285.1:n.320-2784T=
ENST00000680845.1:n.107-30T=
ENST00000681787.1:n.106+12226T=
ENST00000681940.1:n.106+12226T=
ENST00000383070.2:c.*24A= MANE Select ENSP00000372547.1:n.*24A=
ENST00000383070.1:c.*24A= ENSP00000372547.1:n.*24A=
NM_003140.2:c.*24A= NP_003131.1:n.*24A=
NM_003140.3:c.*24A= MANE Select NP_003131.1:n.*24A=