Canonical Allele Identifier: CA2573159669
Gene: SRY HGNC NCBI

Linked Data

dbSNP Id: rs2124486110

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2787313_2787314insG , CM000686.2:g.2787313_2787314insG GRCh38
NC_000024.9:g.2655354_2655355insG , CM000686.1:g.2655354_2655355insG GRCh37
NC_000024.8:g.2715354_2715355insG NCBI36
NG_011751.1:g.5438_5439insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000679518.1:n.106+12574_106+12575insG
ENST00000679825.1:n.425_426insG
ENST00000680285.1:n.320-2436_320-2435insG
ENST00000680845.1:n.166-167_166-166insG
ENST00000681787.1:n.106+12574_106+12575insG
ENST00000681940.1:n.106+12574_106+12575insG
ENST00000383070.2:c.290_291insC MANE Select ENSP00000372547.1:p.Gln97HisfsTer7
ENST00000383070.1:c.290_291insC ENSP00000372547.1:p.Gln97HisfsTer7
NM_003140.2:c.290_291insC NP_003131.1:p.Gln97HisfsTer7
NM_003140.3:c.290_291insC MANE Select NP_003131.1:p.Gln97HisfsTer7