Canonical Allele Identifier: CA1435772857

Gene: WFS1

Linked Data

• dbSNP Id: rs1730986195

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302482_6302507del , CM000666.2:g.6302482_6302507del	GRCh38
NC_000004.11:g.6304209_6304234del , CM000666.1:g.6304209_6304234del	GRCh37
NC_000004.10:g.6355110_6355135del	NCBI36
NG_011700.1:g.37633_37658del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*14_*39del	ENSP00000507852.1:n.*14_*39del
ENST00000683395.1:c.2664_2689del
ENST00000684087.1:c.*14_*39del	ENSP00000506978.1:n.*14_*39del
ENST00000506362.2:c.*14_*39del	ENSP00000424103.2:n.*14_*39del
ENST00000673991.1:c.*14_*39del	ENSP00000501033.1:n.*14_*39del
ENST00000226760.5:c.*14_*39del MANE Select	ENSP00000226760.1:n.*14_*39del
ENST00000503569.5:c.*14_*39del	ENSP00000423337.1:n.*14_*39del
ENST00000507765.1:n.2872_2897del
NM_001145853.1:c.*14_*39del	NP_001139325.1:n.*14_*39del
NM_006005.3:c.*14_*39del MANE Select	NP_005996.2:n.*14_*39del
XM_017008586.1:c.*14_*39del	XP_016864075.1:n.*14_*39del