Canonical Allele Identifier: CA2760271274
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6303044del , CM000666.2:g.6303044del GRCh38
NC_000004.11:g.6304771del , CM000666.1:g.6304771del GRCh37
NC_000004.10:g.6355672del NCBI36
NG_011700.1:g.38195del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.*576del ENSP00000507852.1:n.*576del
ENST00000683395.1:c.3226del
ENST00000684087.1:c.*576del ENSP00000506978.1:n.*576del
ENST00000673991.1:c.*576del ENSP00000501033.1:n.*576del
ENST00000226760.5:c.*576del MANE Select ENSP00000226760.1:n.*576del
ENST00000507765.1:n.3434del
NM_001145853.1:c.*576del NP_001139325.1:n.*576del
NM_006005.3:c.*576del MANE Select NP_005996.2:n.*576del
XM_017008586.1:c.*576del XP_016864075.1:n.*576del
XR_001741566.2:n.1903del