Canonical Allele Identifier: CA2760284550

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300481_6300574del , CM000666.2:g.6300481_6300574del	GRCh38
NC_000004.11:g.6302208_6302301del , CM000666.1:g.6302208_6302301del	GRCh37
NC_000004.10:g.6353109_6353202del	NCBI36
NG_011700.1:g.35632_35725del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.898-176_898-83del	ENSP00000507852.1:n.898-176_898-83del
ENST00000683395.1:c.839-176_839-83del
ENST00000684087.1:c.862-176_862-83del	ENSP00000506978.1:n.862-176_862-83del
ENST00000506362.2:c.613-176_613-83del	ENSP00000424103.2:n.613-176_613-83del
ENST00000673642.1:c.661-316_661-223del	ENSP00000501242.1:n.661-316_661-223del
ENST00000673991.1:c.898-176_898-83del	ENSP00000501033.1:n.898-176_898-83del
ENST00000226760.5:c.862-176_862-83del MANE Select	ENSP00000226760.1:n.862-176_862-83del
ENST00000503569.5:c.862-176_862-83del	ENSP00000423337.1:n.862-176_862-83del
ENST00000506362.1:c.495-176_495-83del
ENST00000507765.1:n.1047-176_1047-83del
ENST00000513395.1:n.420-176_420-83del
NM_001145853.1:c.862-176_862-83del	NP_001139325.1:n.862-176_862-83del
NM_006005.3:c.862-176_862-83del MANE Select	NP_005996.2:n.862-176_862-83del
XM_017008586.1:c.871-176_871-83del	XP_016864075.1:n.871-176_871-83del