Canonical Allele Identifier: CA438211480

Gene: WFS1

Linked Data

• gnomAD v4: 4-6300740-G-C
• MyVariant Identifiers: chr4:g.6302467G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300740G>C , CM000666.2:g.6300740G>C	GRCh38
NC_000004.11:g.6302467G>C , CM000666.1:g.6302467G>C	GRCh37
NC_000004.10:g.6353368G>C	NCBI36
NG_011700.1:g.35891G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.981G>C	ENSP00000507852.1:p.Leu327=
ENST00000683395.1:c.922G>C
ENST00000684087.1:c.945G>C	ENSP00000506978.1:p.Leu315=
ENST00000506362.2:c.696G>C	ENSP00000424103.2:p.Leu232=
ENST00000673642.1:c.661-57G>C	ENSP00000501242.1:n.661-57G>C
ENST00000673991.1:c.981G>C	ENSP00000501033.1:p.Leu327=
ENST00000226760.5:c.945G>C MANE Select	ENSP00000226760.1:p.Leu315=
ENST00000503569.5:c.945G>C	ENSP00000423337.1:p.Leu315=
ENST00000506362.1:c.578G>C
ENST00000507765.1:n.1130G>C
ENST00000513395.1:n.503G>C
NM_001145853.1:c.945G>C	NP_001139325.1:p.Leu315=
NM_006005.3:c.945G>C MANE Select	NP_005996.2:p.Leu315=
XM_017008586.1:c.954G>C	XP_016864075.1:p.Leu318=