Canonical Allele Identifier: CA2760284568

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300575_6300589del , CM000666.2:g.6300575_6300589del	GRCh38
NC_000004.11:g.6302302_6302316del , CM000666.1:g.6302302_6302316del	GRCh37
NC_000004.10:g.6353203_6353217del	NCBI36
NG_011700.1:g.35726_35740del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.898-82_898-68del	ENSP00000507852.1:n.898-82_898-68del
ENST00000683395.1:c.839-82_839-68del
ENST00000684087.1:c.862-82_862-68del	ENSP00000506978.1:n.862-82_862-68del
ENST00000506362.2:c.613-82_613-68del	ENSP00000424103.2:n.613-82_613-68del
ENST00000673642.1:c.661-222_661-208del	ENSP00000501242.1:n.661-222_661-208del
ENST00000673991.1:c.898-82_898-68del	ENSP00000501033.1:n.898-82_898-68del
ENST00000226760.5:c.862-82_862-68del MANE Select	ENSP00000226760.1:n.862-82_862-68del
ENST00000503569.5:c.862-82_862-68del	ENSP00000423337.1:n.862-82_862-68del
ENST00000506362.1:c.495-82_495-68del
ENST00000507765.1:n.1047-82_1047-68del
ENST00000513395.1:n.420-82_420-68del
NM_001145853.1:c.862-82_862-68del	NP_001139325.1:n.862-82_862-68del
NM_006005.3:c.862-82_862-68del MANE Select	NP_005996.2:n.862-82_862-68del
XM_017008586.1:c.871-82_871-68del	XP_016864075.1:n.871-82_871-68del