Canonical Allele Identifier: CA2669843749

Gene: WFS1

Linked Data

• gnomAD v4: 4-6302703-T-TGAGC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302704_6302707dup , CM000666.2:g.6302704_6302707dup	GRCh38
NC_000004.11:g.6304431_6304434dup , CM000666.1:g.6304431_6304434dup	GRCh37
NC_000004.10:g.6355332_6355335dup	NCBI36
NG_011700.1:g.37855_37858dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*236_*239dup	ENSP00000507852.1:n.*236_*239dup
ENST00000683395.1:c.2886_2889dup
ENST00000684087.1:c.*236_*239dup	ENSP00000506978.1:n.*236_*239dup
ENST00000506362.2:c.*236_*239dup	ENSP00000424103.2:n.*236_*239dup
ENST00000673991.1:c.*236_*239dup	ENSP00000501033.1:n.*236_*239dup
ENST00000226760.5:c.*236_*239dup MANE Select	ENSP00000226760.1:n.*236_*239dup
ENST00000503569.5:c.*236_*239dup	ENSP00000423337.1:n.*236_*239dup
ENST00000507765.1:n.3094_3097dup
NM_001145853.1:c.*236_*239dup	NP_001139325.1:n.*236_*239dup
NM_006005.3:c.*236_*239dup MANE Select	NP_005996.2:n.*236_*239dup
XM_017008586.1:c.*236_*239dup	XP_016864075.1:n.*236_*239dup