Canonical Allele Identifier: CA2669843502
Gene: WFS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302510_6302525del , CM000666.2:g.6302510_6302525del GRCh38
NC_000004.11:g.6304237_6304252del , CM000666.1:g.6304237_6304252del GRCh37
NC_000004.10:g.6355138_6355153del NCBI36
NG_011700.1:g.37661_37676del

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.*42_*57del ENSP00000507852.1:n.*42_*57del
ENST00000683395.1:c.2692_2707del
ENST00000684087.1:c.*42_*57del ENSP00000506978.1:n.*42_*57del
ENST00000506362.2:c.*42_*57del ENSP00000424103.2:n.*42_*57del
ENST00000673991.1:c.*42_*57del ENSP00000501033.1:n.*42_*57del
ENST00000226760.5:c.*42_*57del MANE Select ENSP00000226760.1:n.*42_*57del
ENST00000503569.5:c.*42_*57del ENSP00000423337.1:n.*42_*57del
ENST00000507765.1:n.2900_2915del
NM_001145853.1:c.*42_*57del NP_001139325.1:n.*42_*57del
NM_006005.3:c.*42_*57del MANE Select NP_005996.2:n.*42_*57del
XM_017008586.1:c.*42_*57del XP_016864075.1:n.*42_*57del