Canonical Allele Identifier: CA2760271272
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6303010_6303014del , CM000666.2:g.6303010_6303014del GRCh38
NC_000004.11:g.6304737_6304741del , CM000666.1:g.6304737_6304741del GRCh37
NC_000004.10:g.6355638_6355642del NCBI36
NG_011700.1:g.38161_38165del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.*542_*546del ENSP00000507852.1:n.*542_*546del
ENST00000683395.1:c.3192_3196del
ENST00000684087.1:c.*542_*546del ENSP00000506978.1:n.*542_*546del
ENST00000673991.1:c.*542_*546del ENSP00000501033.1:n.*542_*546del
ENST00000226760.5:c.*542_*546del MANE Select ENSP00000226760.1:n.*542_*546del
ENST00000507765.1:n.3400_3404del
NM_001145853.1:c.*542_*546del NP_001139325.1:n.*542_*546del
NM_006005.3:c.*542_*546del MANE Select NP_005996.2:n.*542_*546del
XM_017008586.1:c.*542_*546del XP_016864075.1:n.*542_*546del
XR_001741566.2:n.1931_1935del