Canonical Allele Identifier: CA1435768466
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs1553876863

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6291022_6291023insAGTGGCAGGGG , CM000666.2:g.6291022_6291023insAGTGGCAGGGG GRCh38
NC_000004.11:g.6292749_6292750insAGTGGCAGGGG , CM000666.1:g.6292749_6292750insAGTGGCAGGGG GRCh37
NC_000004.10:g.6343650_6343651insAGTGGCAGGGG NCBI36
NG_011700.1:g.26173_26174insAGTGGCAGGGG

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.461-175_461-174insAGTGGCAGGGG ENSP00000507852.1:n.461-175_461-174insAGT...
ENST00000683395.1:c.451-175_451-174insAGTGGCAGGGG
ENST00000684087.1:c.461-175_461-174insAGTGGCAGGGG ENSP00000506978.1:n.461-175_461-174insAGT...
ENST00000684700.1:c.461-175_461-174insAGTGGCAGGGG ENSP00000507806.1:n.461-175_461-174insAGT...
ENST00000506362.2:c.212-175_212-174insAGTGGCAGGGG ENSP00000424103.2:n.212-175_212-174insAGT...
ENST00000673642.1:c.260-175_260-174insAGTGGCAGGGG ENSP00000501242.1:n.260-175_260-174insAGT...
ENST00000673991.1:c.461-175_461-174insAGTGGCAGGGG ENSP00000501033.1:n.461-175_461-174insAGT...
ENST00000674051.1:c.335-175_335-174insAGTGGCAGGGG ENSP00000501083.1:n.335-175_335-174insAGT...
ENST00000226760.5:c.461-175_461-174insAGTGGCAGGGG MANE Select ENSP00000226760.1:n.461-175_461-174insAGT...
ENST00000503569.5:c.461-175_461-174insAGTGGCAGGGG ENSP00000423337.1:n.461-175_461-174insAGT...
ENST00000506362.1:c.58-175_58-174insAGTGGCAGGGG
ENST00000507765.1:n.646-175_646-174insAGTGGCAGGGG
NM_001145853.1:c.461-175_461-174insAGTGGCAGGGG NP_001139325.1:n.461-175_461-174insAGTGGC...
NM_006005.3:c.461-175_461-174insAGTGGCAGGGG MANE Select NP_005996.2:n.461-175_461-174insAGTGGCAGG...
XM_017008586.1:c.470-175_470-174insAGTGGCAGGGG XP_016864075.1:n.470-175_470-174insAGTGGC...