Canonical Allele Identifier: CA2580071757
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2434653
ClinVar RCV Id: RCV003131902

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6300685_6300732dup , CM000666.2:g.6300685_6300732dup GRCh38
NC_000004.11:g.6302412_6302459dup , CM000666.1:g.6302412_6302459dup GRCh37
NC_000004.10:g.6353313_6353360dup NCBI36
NG_011700.1:g.35836_35883dup

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.926_973dup ENSP00000507852.1:p.Met324_His325insLeuGl...
ENST00000683395.1:c.867_914dup
ENST00000684087.1:c.890_937dup ENSP00000506978.1:p.Met312_His313insLeuGl...
ENST00000506362.2:c.641_688dup ENSP00000424103.2:p.Met229_His230insLeuGl...
ENST00000673642.1:c.661-112_661-65dup ENSP00000501242.1:n.661-112_661-65dup
ENST00000673991.1:c.926_973dup ENSP00000501033.1:p.Met324_His325insLeuGl...
ENST00000226760.5:c.890_937dup MANE Select ENSP00000226760.1:p.Met312_His313insLeuGl...
ENST00000503569.5:c.890_937dup ENSP00000423337.1:p.Met312_His313insLeuGl...
ENST00000506362.1:c.523_570dup
ENST00000507765.1:n.1075_1122dup
ENST00000513395.1:n.448_495dup
NM_001145853.1:c.890_937dup NP_001139325.1:p.Met312_His313insLeuGluIl...
NM_006005.3:c.890_937dup MANE Select NP_005996.2:p.Met312_His313insLeuGluIleLy...
XM_017008586.1:c.899_946dup XP_016864075.1:p.Met315_His316insLeuGluIl...