Canonical Allele Identifier: CA917120752

Gene: WFS1

Linked Data

• dbSNP Id: rs1578614387

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302855_6302865del , CM000666.2:g.6302855_6302865del	GRCh38
NC_000004.11:g.6304582_6304592del , CM000666.1:g.6304582_6304592del	GRCh37
NC_000004.10:g.6355483_6355493del	NCBI36
NG_011700.1:g.38006_38016del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*387_*397del	ENSP00000507852.1:n.*387_*397del
ENST00000683395.1:c.3037_3047del
ENST00000684087.1:c.*387_*397del	ENSP00000506978.1:n.*387_*397del
ENST00000506362.2:c.*387_*397del	ENSP00000424103.2:n.*387_*397del
ENST00000673991.1:c.*387_*397del	ENSP00000501033.1:n.*387_*397del
ENST00000226760.5:c.*387_*397del MANE Select	ENSP00000226760.1:n.*387_*397del
ENST00000503569.5:c.*387_*397del	ENSP00000423337.1:n.*387_*397del
ENST00000507765.1:n.3245_3255del
NM_001145853.1:c.*387_*397del	NP_001139325.1:n.*387_*397del
NM_006005.3:c.*387_*397del MANE Select	NP_005996.2:n.*387_*397del
XM_017008586.1:c.*387_*397del	XP_016864075.1:n.*387_*397del