Canonical Allele Identifier: CA1435771686

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300465_6300467delinsCAG , CM000666.2:g.6300465_6300467delinsCAG	GRCh38
NC_000004.11:g.6302192_6302194delinsCAG , CM000666.1:g.6302192_6302194delinsCAG	GRCh37
NC_000004.10:g.6353093_6353095delinsCAG	NCBI36
NG_011700.1:g.35616_35618delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.898-192_898-190delinsCAG	ENSP00000507852.1:n.898-192_898-190delinsCAG
ENST00000683395.1:c.839-192_839-190delinsCAG
ENST00000684087.1:c.862-192_862-190delinsCAG	ENSP00000506978.1:n.862-192_862-190delinsCAG
ENST00000506362.2:c.613-192_613-190delinsCAG	ENSP00000424103.2:n.613-192_613-190delinsCAG
ENST00000673642.1:c.661-332_661-330delinsCAG	ENSP00000501242.1:n.661-332_661-330delinsCAG
ENST00000673991.1:c.898-192_898-190delinsCAG	ENSP00000501033.1:n.898-192_898-190delinsCAG
ENST00000226760.5:c.862-192_862-190delinsCAG MANE Select	ENSP00000226760.1:n.862-192_862-190delinsCAG
ENST00000503569.5:c.862-192_862-190delinsCAG	ENSP00000423337.1:n.862-192_862-190delinsCAG
ENST00000506362.1:c.495-192_495-190delinsCAG
ENST00000507765.1:n.1047-192_1047-190delinsCAG
ENST00000513395.1:n.420-192_420-190delinsCAG
NM_001145853.1:c.862-192_862-190delinsCAG	NP_001139325.1:n.862-192_862-190delinsCAG
NM_006005.3:c.862-192_862-190delinsCAG MANE Select	NP_005996.2:n.862-192_862-190delinsCAG
XM_017008586.1:c.871-192_871-190delinsCAG	XP_016864075.1:n.871-192_871-190delinsCAG