Canonical Allele Identifier: CA2760284538

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300435_6300456dup , CM000666.2:g.6300435_6300456dup	GRCh38
NC_000004.11:g.6302162_6302183dup , CM000666.1:g.6302162_6302183dup	GRCh37
NC_000004.10:g.6353063_6353084dup	NCBI36
NG_011700.1:g.35586_35607dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.898-222_898-201dup	ENSP00000507852.1:n.898-222_898-201dup
ENST00000683395.1:c.839-222_839-201dup
ENST00000684087.1:c.862-222_862-201dup	ENSP00000506978.1:n.862-222_862-201dup
ENST00000506362.2:c.613-222_613-201dup	ENSP00000424103.2:n.613-222_613-201dup
ENST00000673642.1:c.661-362_661-341dup	ENSP00000501242.1:n.661-362_661-341dup
ENST00000673991.1:c.898-222_898-201dup	ENSP00000501033.1:n.898-222_898-201dup
ENST00000226760.5:c.862-222_862-201dup MANE Select	ENSP00000226760.1:n.862-222_862-201dup
ENST00000503569.5:c.862-222_862-201dup	ENSP00000423337.1:n.862-222_862-201dup
ENST00000506362.1:c.495-222_495-201dup
ENST00000507765.1:n.1047-222_1047-201dup
ENST00000513395.1:n.420-222_420-201dup
NM_001145853.1:c.862-222_862-201dup	NP_001139325.1:n.862-222_862-201dup
NM_006005.3:c.862-222_862-201dup MANE Select	NP_005996.2:n.862-222_862-201dup
XM_017008586.1:c.871-222_871-201dup	XP_016864075.1:n.871-222_871-201dup