Canonical Allele Identifier: CA1435773043
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs1730998331

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302632_6302633insACCATGTGTAGATT , CM000666.2:g.6302632_6302633insACCATGTGTAGATT GRCh38
NC_000004.11:g.6304359_6304360insACCATGTGTAGATT , CM000666.1:g.6304359_6304360insACCATGTGTAGATT GRCh37
NC_000004.10:g.6355260_6355261insACCATGTGTAGATT NCBI36
NG_011700.1:g.37783_37784insACCATGTGTAGATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.*164_*165insACCATGTGTAGATT ENSP00000507852.1:n.*164_*165insACCATGTGTAGATT
ENST00000683395.1:c.2814_2815insACCATGTGTAGATT
ENST00000684087.1:c.*164_*165insACCATGTGTAGATT ENSP00000506978.1:n.*164_*165insACCATGTGTAGATT
ENST00000506362.2:c.*164_*165insACCATGTGTAGATT ENSP00000424103.2:n.*164_*165insACCATGTGTAGATT
ENST00000673991.1:c.*164_*165insACCATGTGTAGATT ENSP00000501033.1:n.*164_*165insACCATGTGTAGATT
ENST00000226760.5:c.*164_*165insACCATGTGTAGATT MANE Select ENSP00000226760.1:n.*164_*165insACCATGTGTAGATT
ENST00000503569.5:c.*164_*165insACCATGTGTAGATT ENSP00000423337.1:n.*164_*165insACCATGTGTAGATT
ENST00000507765.1:n.3022_3023insACCATGTGTAGATT
NM_001145853.1:c.*164_*165insACCATGTGTAGATT NP_001139325.1:n.*164_*165insACCATGTGTAGATT
NM_006005.3:c.*164_*165insACCATGTGTAGATT MANE Select NP_005996.2:n.*164_*165insACCATGTGTAGATT
XM_017008586.1:c.*164_*165insACCATGTGTAGATT XP_016864075.1:n.*164_*165insACCATGTGTAGATT