Canonical Allele Identifier: CA438367901

Gene: WFS1

Linked Data

• MyVariant Identifiers: chr4:g.6302563G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300836G>C , CM000666.2:g.6300836G>C	GRCh38
NC_000004.11:g.6302563G>C , CM000666.1:g.6302563G>C	GRCh37
NC_000004.10:g.6353464G>C	NCBI36
NG_011700.1:g.35987G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1077G>C	ENSP00000507852.1:p.Leu359=
ENST00000683395.1:c.1018G>C
ENST00000684087.1:c.1041G>C	ENSP00000506978.1:p.Leu347=
ENST00000506362.2:c.792G>C	ENSP00000424103.2:p.Leu264=
ENST00000673642.1:c.700G>C	ENSP00000501242.1:p.Gly234Arg
ENST00000673991.1:c.1077G>C	ENSP00000501033.1:p.Leu359=
ENST00000226760.5:c.1041G>C MANE Select	ENSP00000226760.1:p.Leu347=
ENST00000503569.5:c.1041G>C	ENSP00000423337.1:p.Leu347=
ENST00000506362.1:c.674G>C
ENST00000507765.1:n.1226G>C
NM_001145853.1:c.1041G>C	NP_001139325.1:p.Leu347=
NM_006005.3:c.1041G>C MANE Select	NP_005996.2:p.Leu347=
XM_017008586.1:c.1050G>C	XP_016864075.1:p.Leu350=