Canonical Allele Identifier: CA2507389804
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6303008dup , CM000666.2:g.6303008dup GRCh38
NC_000004.11:g.6304735dup , CM000666.1:g.6304735dup GRCh37
NC_000004.10:g.6355636dup NCBI36
NG_011700.1:g.38159dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.*540dup ENSP00000507852.1:n.*540dup
ENST00000683395.1:c.3190dup
ENST00000684087.1:c.*540dup ENSP00000506978.1:n.*540dup
ENST00000673991.1:c.*540dup ENSP00000501033.1:n.*540dup
ENST00000226760.5:c.*540dup MANE Select ENSP00000226760.1:n.*540dup
ENST00000507765.1:n.3398dup
NM_001145853.1:c.*540dup NP_001139325.1:n.*540dup
NM_006005.3:c.*540dup MANE Select NP_005996.2:n.*540dup
XM_017008586.1:c.*540dup XP_016864075.1:n.*540dup
XR_001741566.2:n.1941dup