Canonical Allele Identifier: CA1435771676

Gene: WFS1

Linked Data

• dbSNP Id: rs1730836670

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300461_6300469del , CM000666.2:g.6300461_6300469del	GRCh38
NC_000004.11:g.6302188_6302196del , CM000666.1:g.6302188_6302196del	GRCh37
NC_000004.10:g.6353089_6353097del	NCBI36
NG_011700.1:g.35612_35620del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.898-196_898-188del	ENSP00000507852.1:n.898-196_898-188del
ENST00000683395.1:c.839-196_839-188del
ENST00000684087.1:c.862-196_862-188del	ENSP00000506978.1:n.862-196_862-188del
ENST00000506362.2:c.613-196_613-188del	ENSP00000424103.2:n.613-196_613-188del
ENST00000673642.1:c.661-336_661-328del	ENSP00000501242.1:n.661-336_661-328del
ENST00000673991.1:c.898-196_898-188del	ENSP00000501033.1:n.898-196_898-188del
ENST00000226760.5:c.862-196_862-188del MANE Select	ENSP00000226760.1:n.862-196_862-188del
ENST00000503569.5:c.862-196_862-188del	ENSP00000423337.1:n.862-196_862-188del
ENST00000506362.1:c.495-196_495-188del
ENST00000507765.1:n.1047-196_1047-188del
ENST00000513395.1:n.420-196_420-188del
NM_001145853.1:c.862-196_862-188del	NP_001139325.1:n.862-196_862-188del
NM_006005.3:c.862-196_862-188del MANE Select	NP_005996.2:n.862-196_862-188del
XM_017008586.1:c.871-196_871-188del	XP_016864075.1:n.871-196_871-188del