Canonical Allele Identifier: CA797127993

Gene: WFS1

Linked Data

• dbSNP Id: rs1433702159
• MyVariant Identifiers: chr4:g.6293233_6293234del (hg19) ; chr4:g.6291506_6291507del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291506_6291507del , CM000666.2:g.6291506_6291507del	GRCh38
NC_000004.11:g.6293233_6293234del , CM000666.1:g.6293233_6293234del	GRCh37
NC_000004.10:g.6344134_6344135del	NCBI36
NG_011700.1:g.26657_26658del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+139_631+140del	ENSP00000507852.1:n.631+139_631+140del
ENST00000683395.1:c.608+152_608+153del
ENST00000684087.1:c.631+139_631+140del	ENSP00000506978.1:n.631+139_631+140del
ENST00000684700.1:c.*65_*66del	ENSP00000507806.1:n.*65_*66del
ENST00000506362.2:c.382+139_382+140del	ENSP00000424103.2:n.382+139_382+140del
ENST00000673642.1:c.430+139_430+140del	ENSP00000501242.1:n.430+139_430+140del
ENST00000673991.1:c.631+139_631+140del	ENSP00000501033.1:n.631+139_631+140del
ENST00000226760.5:c.631+139_631+140del MANE Select	ENSP00000226760.1:n.631+139_631+140del
ENST00000503569.5:c.631+139_631+140del	ENSP00000423337.1:n.631+139_631+140del
ENST00000506362.1:c.228+139_228+140del
ENST00000507765.1:n.816+139_816+140del
NM_001145853.1:c.631+139_631+140del	NP_001139325.1:n.631+139_631+140del
NM_006005.3:c.631+139_631+140del MANE Select	NP_005996.2:n.631+139_631+140del
XM_017008586.1:c.640+139_640+140del	XP_016864075.1:n.640+139_640+140del