Canonical Allele Identifier: CA91796172

Gene: WFS1

Linked Data

• dbSNP Id: rs894229873
• MyVariant Identifiers: chr4:g.6302208_6302229del (hg19) ; chr4:g.6300481_6300502del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300489_6300510del , CM000666.2:g.6300489_6300510del	GRCh38
NC_000004.11:g.6302216_6302237del , CM000666.1:g.6302216_6302237del	GRCh37
NC_000004.10:g.6353117_6353138del	NCBI36
NG_011700.1:g.35640_35661del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.898-168_898-147del	ENSP00000507852.1:n.898-168_898-147del
ENST00000683395.1:c.839-168_839-147del
ENST00000684087.1:c.862-168_862-147del	ENSP00000506978.1:n.862-168_862-147del
ENST00000506362.2:c.613-168_613-147del	ENSP00000424103.2:n.613-168_613-147del
ENST00000673642.1:c.661-308_661-287del	ENSP00000501242.1:n.661-308_661-287del
ENST00000673991.1:c.898-168_898-147del	ENSP00000501033.1:n.898-168_898-147del
ENST00000226760.5:c.862-168_862-147del MANE Select	ENSP00000226760.1:n.862-168_862-147del
ENST00000503569.5:c.862-168_862-147del	ENSP00000423337.1:n.862-168_862-147del
ENST00000506362.1:c.495-168_495-147del
ENST00000507765.1:n.1047-168_1047-147del
ENST00000513395.1:n.420-168_420-147del
NM_001145853.1:c.862-168_862-147del	NP_001139325.1:n.862-168_862-147del
NM_006005.3:c.862-168_862-147del MANE Select	NP_005996.2:n.862-168_862-147del
XM_017008586.1:c.871-168_871-147del	XP_016864075.1:n.871-168_871-147del