Canonical Allele Identifier: CA1435772252
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6300833G= , CM000666.2:g.6300833G= GRCh38
NC_000004.11:g.6302560G= , CM000666.1:g.6302560G= GRCh37
NC_000004.10:g.6353461G= NCBI36
NG_011700.1:g.35984G=

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.1074G= ENSP00000507852.1:p.Pro358=
ENST00000683395.1:c.1015G=
ENST00000684087.1:c.1038G= ENSP00000506978.1:p.Pro346=
ENST00000506362.2:c.789G= ENSP00000424103.2:p.Pro263=
ENST00000673642.1:c.697G= ENSP00000501242.1:p.Ala233=
ENST00000673991.1:c.1074G= ENSP00000501033.1:p.Pro358=
ENST00000226760.5:c.1038G= MANE Select ENSP00000226760.1:p.Pro346=
ENST00000503569.5:c.1038G= ENSP00000423337.1:p.Pro346=
ENST00000506362.1:c.671G=
ENST00000507765.1:n.1223G=
NM_001145853.1:c.1038G= NP_001139325.1:p.Pro346=
NM_006005.3:c.1038G= MANE Select NP_005996.2:p.Pro346=
XM_017008586.1:c.1047G= XP_016864075.1:p.Pro349=