Canonical Allele Identifier: CA1058893141
Gene: WFS1 HGNC NCBI

Linked Data

gnomAD v3: 4-6302626-G-GT
gnomAD v4: 4-6302626-G-GT

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302626_6302627insT , CM000666.2:g.6302626_6302627insT GRCh38
NC_000004.11:g.6304353_6304354insT , CM000666.1:g.6304353_6304354insT GRCh37
NC_000004.10:g.6355254_6355255insT NCBI36
NG_011700.1:g.37777_37778insT

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.*158_*159insT ENSP00000507852.1:n.*158_*159insT
ENST00000683395.1:c.2808_2809insT
ENST00000684087.1:c.*158_*159insT ENSP00000506978.1:n.*158_*159insT
ENST00000506362.2:c.*158_*159insT ENSP00000424103.2:n.*158_*159insT
ENST00000673991.1:c.*158_*159insT ENSP00000501033.1:n.*158_*159insT
ENST00000226760.5:c.*158_*159insT MANE Select ENSP00000226760.1:n.*158_*159insT
ENST00000503569.5:c.*158_*159insT ENSP00000423337.1:n.*158_*159insT
ENST00000507765.1:n.3016_3017insT
NM_001145853.1:c.*158_*159insT NP_001139325.1:n.*158_*159insT
NM_006005.3:c.*158_*159insT MANE Select NP_005996.2:n.*158_*159insT
XM_017008586.1:c.*158_*159insT XP_016864075.1:n.*158_*159insT