Canonical Allele Identifier: CA797212333

Gene: WFS1

Linked Data

• dbSNP Id: rs1191893106
• MyVariant Identifiers: chr4:g.6304752_6304753del (hg19) ; chr4:g.6303025_6303026del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6303029_6303030del , CM000666.2:g.6303029_6303030del	GRCh38
NC_000004.11:g.6304756_6304757del , CM000666.1:g.6304756_6304757del	GRCh37
NC_000004.10:g.6355657_6355658del	NCBI36
NG_011700.1:g.38180_38181del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*561_*562del	ENSP00000507852.1:n.*561_*562del
ENST00000683395.1:c.3211_3212del
ENST00000684087.1:c.*561_*562del	ENSP00000506978.1:n.*561_*562del
ENST00000673991.1:c.*561_*562del	ENSP00000501033.1:n.*561_*562del
ENST00000226760.5:c.*561_*562del MANE Select	ENSP00000226760.1:n.*561_*562del
ENST00000507765.1:n.3419_3420del
NM_001145853.1:c.*561_*562del	NP_001139325.1:n.*561_*562del
NM_006005.3:c.*561_*562del MANE Select	NP_005996.2:n.*561_*562del
XM_017008586.1:c.*561_*562del	XP_016864075.1:n.*561_*562del
XR_001741566.2:n.1919_1920del