Canonical Allele Identifier: CA2578035826
Gene: WFS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302510_6302517dup , CM000666.2:g.6302510_6302517dup GRCh38
NC_000004.11:g.6304237_6304244dup , CM000666.1:g.6304237_6304244dup GRCh37
NC_000004.10:g.6355138_6355145dup NCBI36
NG_011700.1:g.37661_37668dup

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.*42_*49dup ENSP00000507852.1:n.*42_*49dup
ENST00000683395.1:c.2692_2699dup
ENST00000684087.1:c.*42_*49dup ENSP00000506978.1:n.*42_*49dup
ENST00000506362.2:c.*42_*49dup ENSP00000424103.2:n.*42_*49dup
ENST00000673991.1:c.*42_*49dup ENSP00000501033.1:n.*42_*49dup
ENST00000226760.5:c.*42_*49dup MANE Select ENSP00000226760.1:n.*42_*49dup
ENST00000503569.5:c.*42_*49dup ENSP00000423337.1:n.*42_*49dup
ENST00000507765.1:n.2900_2907dup
NM_001145853.1:c.*42_*49dup NP_001139325.1:n.*42_*49dup
NM_006005.3:c.*42_*49dup MANE Select NP_005996.2:n.*42_*49dup
XM_017008586.1:c.*42_*49dup XP_016864075.1:n.*42_*49dup