Canonical Allele Identifier: CA797212182
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs960431689

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302903_6302906dup , CM000666.2:g.6302903_6302906dup GRCh38
NC_000004.11:g.6304630_6304633dup , CM000666.1:g.6304630_6304633dup GRCh37
NC_000004.10:g.6355531_6355534dup NCBI36
NG_011700.1:g.38054_38057dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.*435_*438dup ENSP00000507852.1:n.*435_*438dup
ENST00000683395.1:c.3085_3088dup
ENST00000684087.1:c.*435_*438dup ENSP00000506978.1:n.*435_*438dup
ENST00000673991.1:c.*435_*438dup ENSP00000501033.1:n.*435_*438dup
ENST00000226760.5:c.*435_*438dup MANE Select ENSP00000226760.1:n.*435_*438dup
ENST00000507765.1:n.3293_3296dup
NM_001145853.1:c.*435_*438dup NP_001139325.1:n.*435_*438dup
NM_006005.3:c.*435_*438dup MANE Select NP_005996.2:n.*435_*438dup
XM_017008586.1:c.*435_*438dup XP_016864075.1:n.*435_*438dup
XR_001741566.2:n.2043_2046dup