Canonical Allele Identifier: CA1435771782

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300543_6300559delinsACGCAAGGGTGCGGGTT , CM000666.2:g.6300543_6300559delinsACGCAAGGGTGCGGGTT	GRCh38
NC_000004.11:g.6302270_6302286delinsACGCAAGGGTGCGGGTT , CM000666.1:g.6302270_6302286delinsACGCAAGGGTGCGGGTT	GRCh37
NC_000004.10:g.6353171_6353187delinsACGCAAGGGTGCGGGTT	NCBI36
NG_011700.1:g.35694_35710delinsACGCAAGGGTGCGGGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.898-114_898-98delinsACGCAAGGGTGCGGGTT	ENSP00000507852.1:n.898-114_898-98delinsACGCAAGGGTGCGGGTT
ENST00000683395.1:c.839-114_839-98delinsACGCAAGGGTGCGGGTT
ENST00000684087.1:c.862-114_862-98delinsACGCAAGGGTGCGGGTT	ENSP00000506978.1:n.862-114_862-98delinsACGCAAGGGTGCGGGTT
ENST00000506362.2:c.613-114_613-98delinsACGCAAGGGTGCGGGTT	ENSP00000424103.2:n.613-114_613-98delinsACGCAAGGGTGCGGGTT
ENST00000673642.1:c.661-254_661-238delinsACGCAAGGGTGCGGGTT	ENSP00000501242.1:n.661-254_661-238delinsACGCAAGGGTGCGGGTT
ENST00000673991.1:c.898-114_898-98delinsACGCAAGGGTGCGGGTT	ENSP00000501033.1:n.898-114_898-98delinsACGCAAGGGTGCGGGTT
ENST00000226760.5:c.862-114_862-98delinsACGCAAGGGTGCGGGTT MANE Select	ENSP00000226760.1:n.862-114_862-98delinsACGCAAGGGTGCGGGTT
ENST00000503569.5:c.862-114_862-98delinsACGCAAGGGTGCGGGTT	ENSP00000423337.1:n.862-114_862-98delinsACGCAAGGGTGCGGGTT
ENST00000506362.1:c.495-114_495-98delinsACGCAAGGGTGCGGGTT
ENST00000507765.1:n.1047-114_1047-98delinsACGCAAGGGTGCGGGTT
ENST00000513395.1:n.420-114_420-98delinsACGCAAGGGTGCGGGTT
NM_001145853.1:c.862-114_862-98delinsACGCAAGGGTGCGGGTT	NP_001139325.1:n.862-114_862-98delinsACGCAAGGGTGCGGGTT
NM_006005.3:c.862-114_862-98delinsACGCAAGGGTGCGGGTT MANE Select	NP_005996.2:n.862-114_862-98delinsACGCAAGGGTGCGGGTT
XM_017008586.1:c.871-114_871-98delinsACGCAAGGGTGCGGGTT	XP_016864075.1:n.871-114_871-98delinsACGCAAGGGTGCGGGTT