Canonical Allele Identifier: CA648122080
Gene: WFS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302721_6302722insA , CM000666.2:g.6302721_6302722insA GRCh38
NC_000004.11:g.6304448_6304449insA , CM000666.1:g.6304448_6304449insA GRCh37
NC_000004.10:g.6355349_6355350insA NCBI36
NG_011700.1:g.37872_37873insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.*253_*254insA ENSP00000507852.1:n.*253_*254insA
ENST00000683395.1:c.2903_2904insA
ENST00000684087.1:c.*253_*254insA ENSP00000506978.1:n.*253_*254insA
ENST00000506362.2:c.*253_*254insA ENSP00000424103.2:n.*253_*254insA
ENST00000673991.1:c.*253_*254insA ENSP00000501033.1:n.*253_*254insA
ENST00000226760.5:c.*253_*254insA MANE Select ENSP00000226760.1:n.*253_*254insA
ENST00000503569.5:c.*253_*254insA ENSP00000423337.1:n.*253_*254insA
ENST00000507765.1:n.3111_3112insA
NM_001145853.1:c.*253_*254insA NP_001139325.1:n.*253_*254insA
NM_006005.3:c.*253_*254insA MANE Select NP_005996.2:n.*253_*254insA
XM_017008586.1:c.*253_*254insA XP_016864075.1:n.*253_*254insA