Canonical Allele Identifier: CA2586973594

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291268_6291273del , CM000666.2:g.6291268_6291273del	GRCh38
NC_000004.11:g.6292995_6293000del , CM000666.1:g.6292995_6293000del	GRCh37
NC_000004.10:g.6343896_6343901del	NCBI36
NG_011700.1:g.26419_26424del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.532_537del	ENSP00000507852.1:p.Lys178_Ala179del
ENST00000683395.1:c.522_527del
ENST00000684087.1:c.532_537del	ENSP00000506978.1:p.Lys178_Ala179del
ENST00000684700.1:c.532_537del	ENSP00000507806.1:p.Lys178_Ala179del
ENST00000506362.2:c.283_288del	ENSP00000424103.2:p.Lys95_Ala96del
ENST00000673642.1:c.331_336del	ENSP00000501242.1:p.Lys111_Ala112del
ENST00000673991.1:c.532_537del	ENSP00000501033.1:p.Lys178_Ala179del
ENST00000674051.1:c.406_411del	ENSP00000501083.1:p.Lys136_Ala137del
ENST00000226760.5:c.532_537del MANE Select	ENSP00000226760.1:p.Lys178_Ala179del
ENST00000503569.5:c.532_537del	ENSP00000423337.1:p.Lys178_Ala179del
ENST00000506362.1:c.129_134del
ENST00000507765.1:n.717_722del
NM_001145853.1:c.532_537del	NP_001139325.1:p.Lys178_Ala179del
NM_006005.3:c.532_537del MANE Select	NP_005996.2:p.Lys178_Ala179del
XM_017008586.1:c.541_546del	XP_016864075.1:p.Lys181_Ala182del