Canonical Allele Identifier: CA116905
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 4527
dbSNP Id: rs10010131

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6291188A>G , CM000666.2:g.6291188A>G GRCh38
NC_000004.11:g.6292915A>G , CM000666.1:g.6292915A>G GRCh37
NC_000004.10:g.6343816A>G NCBI36
NG_011700.1:g.26339A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.461-9A>G ENSP00000507852.1:n.461-9A>G
ENST00000683395.1:n.451-9A>G
ENST00000684087.1:c.461-9A>G ENSP00000506978.1:n.461-9A>G
ENST00000684700.1:c.461-9A>G ENSP00000507806.1:n.461-9A>G
ENST00000506362.2:c.212-9A>G ENSP00000424103.2:n.212-9A>G
ENST00000673642.1:n.260-9A>G ENSP00000501242.1:n.260-9A>G
ENST00000673991.1:c.461-9A>G ENSP00000501033.1:n.461-9A>G
ENST00000674051.1:c.335-9A>G ENSP00000501083.1:n.335-9A>G
ENST00000226760.5:c.461-9A>G MANE Select ENSP00000226760.1:n.461-9A>G
ENST00000503569.5:c.461-9A>G ENSP00000423337.1:n.461-9A>G
ENST00000506362.1:n.58-9A>G
ENST00000507765.1:n.646-9A>G
NM_001145853.1:c.461-9A>G NP_001139325.1:n.461-9A>G
NM_006005.3:c.461-9A>G MANE Select NP_005996.2:n.461-9A>G
XM_017008586.1:c.470-9A>G XP_016864075.1:n.470-9A>G