Canonical Allele Identifier: CA356176996

Gene: WFS1

Linked Data

• MyVariant Identifiers: chr4:g.6303386G>C (hg19) ; chr4:g.6301659G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301659G>C , CM000666.2:g.6301659G>C	GRCh38
NC_000004.11:g.6303386G>C , CM000666.1:g.6303386G>C	GRCh37
NC_000004.10:g.6354287G>C	NCBI36
NG_011700.1:g.36810G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1900G>C	ENSP00000507852.1:p.Gly634Arg
ENST00000683395.1:c.1841G>C
ENST00000684087.1:c.1864G>C	ENSP00000506978.1:p.Gly622Arg
ENST00000506362.2:c.1615G>C	ENSP00000424103.2:p.Gly539Arg
ENST00000673642.1:c.1523G>C	ENSP00000501242.1:n.1523G>C
ENST00000673991.1:c.1900G>C	ENSP00000501033.1:p.Gly634Arg
ENST00000226760.5:c.1864G>C MANE Select	ENSP00000226760.1:p.Gly622Arg
ENST00000503569.5:c.1864G>C	ENSP00000423337.1:p.Gly622Arg
ENST00000507765.1:n.2049G>C
NM_001145853.1:c.1864G>C	NP_001139325.1:p.Gly622Arg
NM_006005.3:c.1864G>C MANE Select	NP_005996.2:p.Gly622Arg
XM_017008586.1:c.1873G>C	XP_016864075.1:p.Gly625Arg