Canonical Allele Identifier: CA438210958

Gene: WFS1

Linked Data

• MyVariant Identifiers: chr4:g.6292983A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291256A>C , CM000666.2:g.6291256A>C	GRCh38
NC_000004.11:g.6292983A>C , CM000666.1:g.6292983A>C	GRCh37
NC_000004.10:g.6343884A>C	NCBI36
NG_011700.1:g.26407A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.520A>C	ENSP00000507852.1:p.Arg174=
ENST00000683395.1:c.510A>C
ENST00000684087.1:c.520A>C	ENSP00000506978.1:p.Arg174=
ENST00000684700.1:c.520A>C	ENSP00000507806.1:p.Arg174=
ENST00000506362.2:c.271A>C	ENSP00000424103.2:p.Arg91=
ENST00000673642.1:c.319A>C	ENSP00000501242.1:p.Arg107=
ENST00000673991.1:c.520A>C	ENSP00000501033.1:p.Arg174=
ENST00000674051.1:c.394A>C	ENSP00000501083.1:p.Arg132=
ENST00000226760.5:c.520A>C MANE Select	ENSP00000226760.1:p.Arg174=
ENST00000503569.5:c.520A>C	ENSP00000423337.1:p.Arg174=
ENST00000506362.1:c.117A>C
ENST00000507765.1:n.705A>C
NM_001145853.1:c.520A>C	NP_001139325.1:p.Arg174=
NM_006005.3:c.520A>C MANE Select	NP_005996.2:p.Arg174=
XM_017008586.1:c.529A>C	XP_016864075.1:p.Arg177=