Canonical Allele Identifier: CA91797124
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs71526463

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302172_6302174delinsGAG , CM000666.2:g.6302172_6302174delinsGAG GRCh38
NC_000004.11:g.6303899_6303901delinsGAG , CM000666.1:g.6303899_6303901delinsGAG GRCh37
NC_000004.10:g.6354800_6354802delinsGAG NCBI36
NG_011700.1:g.37323_37325delinsGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.2413_2415delinsGAG ENSP00000507852.1:p.Arg805Glu
ENST00000683395.1:c.2354_2356delinsGAG
ENST00000684087.1:c.2377_2379delinsGAG ENSP00000506978.1:p.Arg793Glu
ENST00000506362.2:c.2128_2130delinsGAG ENSP00000424103.2:p.Arg710Glu
ENST00000673991.1:c.2413_2415delinsGAG ENSP00000501033.1:p.Arg805Glu
ENST00000226760.5:c.2377_2379delinsGAG MANE Select ENSP00000226760.1:p.Arg793Glu
ENST00000503569.5:c.2377_2379delinsGAG ENSP00000423337.1:p.Arg793Glu
ENST00000507765.1:n.2562_2564delinsGAG
NM_001145853.1:c.2377_2379delinsGAG NP_001139325.1:p.Arg793Glu
NM_006005.3:c.2377_2379delinsGAG MANE Select NP_005996.2:p.Arg793Glu
XM_017008586.1:c.2386_2388delinsGAG XP_016864075.1:p.Arg796Glu