Canonical Allele Identifier: CA91796164

Gene: WFS1

Linked Data

• dbSNP Id: rs71537684
• MyVariant Identifiers: chr4:g.6302193_6302194del (hg19) ; chr4:g.6300466_6300467del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300466_6300467del , CM000666.2:g.6300466_6300467del	GRCh38
NC_000004.11:g.6302193_6302194del , CM000666.1:g.6302193_6302194del	GRCh37
NC_000004.10:g.6353094_6353095del	NCBI36
NG_011700.1:g.35617_35618del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.898-191_898-190del	ENSP00000507852.1:n.898-191_898-190del
ENST00000683395.1:c.839-191_839-190del
ENST00000684087.1:c.862-191_862-190del	ENSP00000506978.1:n.862-191_862-190del
ENST00000506362.2:c.613-191_613-190del	ENSP00000424103.2:n.613-191_613-190del
ENST00000673642.1:c.661-331_661-330del	ENSP00000501242.1:n.661-331_661-330del
ENST00000673991.1:c.898-191_898-190del	ENSP00000501033.1:n.898-191_898-190del
ENST00000226760.5:c.862-191_862-190del MANE Select	ENSP00000226760.1:n.862-191_862-190del
ENST00000503569.5:c.862-191_862-190del	ENSP00000423337.1:n.862-191_862-190del
ENST00000506362.1:c.495-191_495-190del
ENST00000507765.1:n.1047-191_1047-190del
ENST00000513395.1:n.420-191_420-190del
NM_001145853.1:c.862-191_862-190del	NP_001139325.1:n.862-191_862-190del
NM_006005.3:c.862-191_862-190del MANE Select	NP_005996.2:n.862-191_862-190del
XM_017008586.1:c.871-191_871-190del	XP_016864075.1:n.871-191_871-190del