Canonical Allele Identifier: CA2469659960
Gene: SRY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2787279_2787280delinsAT , CM000686.2:g.2787279_2787280delinsAT GRCh38
NC_000024.9:g.2655320_2655321delinsAT , CM000686.1:g.2655320_2655321delinsAT GRCh37
NC_000024.8:g.2715320_2715321delinsAT NCBI36
NG_011751.1:g.5472_5473delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000679518.1:n.106+12540_106+12541delinsAT
ENST00000679825.1:n.391_392delinsAT
ENST00000680285.1:n.320-2470_320-2469delinsAT
ENST00000680845.1:n.166-201_166-200delinsAT
ENST00000681787.1:n.106+12540_106+12541delinsAT
ENST00000681940.1:n.106+12540_106+12541delinsAT
ENST00000383070.2:c.324_325delinsAT MANE Select ENSP00000372547.1:p.Pro108=
ENST00000383070.1:c.324_325delinsAT ENSP00000372547.1:p.Pro108=
NM_003140.2:c.324_325delinsAT NP_003131.1:p.Pro108=
NM_003140.3:c.324_325delinsAT MANE Select NP_003131.1:p.Pro108=