Canonical Allele Identifier: CA2669843187

Gene: WFS1

Linked Data

• gnomAD v4: 4-6300619-T-TGTCCCAG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300620_6300626dup , CM000666.2:g.6300620_6300626dup	GRCh38
NC_000004.11:g.6302347_6302353dup , CM000666.1:g.6302347_6302353dup	GRCh37
NC_000004.10:g.6353248_6353254dup	NCBI36
NG_011700.1:g.35771_35777dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.898-37_898-31dup	ENSP00000507852.1:n.898-37_898-31dup
ENST00000683395.1:c.839-37_839-31dup
ENST00000684087.1:c.862-37_862-31dup	ENSP00000506978.1:n.862-37_862-31dup
ENST00000506362.2:c.613-37_613-31dup	ENSP00000424103.2:n.613-37_613-31dup
ENST00000673642.1:c.661-177_661-171dup	ENSP00000501242.1:n.661-177_661-171dup
ENST00000673991.1:c.898-37_898-31dup	ENSP00000501033.1:n.898-37_898-31dup
ENST00000226760.5:c.862-37_862-31dup MANE Select	ENSP00000226760.1:n.862-37_862-31dup
ENST00000503569.5:c.862-37_862-31dup	ENSP00000423337.1:n.862-37_862-31dup
ENST00000506362.1:c.495-37_495-31dup
ENST00000507765.1:n.1047-37_1047-31dup
ENST00000513395.1:n.420-37_420-31dup
NM_001145853.1:c.862-37_862-31dup	NP_001139325.1:n.862-37_862-31dup
NM_006005.3:c.862-37_862-31dup MANE Select	NP_005996.2:n.862-37_862-31dup
XM_017008586.1:c.871-37_871-31dup	XP_016864075.1:n.871-37_871-31dup