Canonical Allele Identifier: CA438369080

Gene: WFS1

Linked Data

• gnomAD v4: 4-6301535-G-C
• MyVariant Identifiers: chr4:g.6303262G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301535G>C , CM000666.2:g.6301535G>C	GRCh38
NC_000004.11:g.6303262G>C , CM000666.1:g.6303262G>C	GRCh37
NC_000004.10:g.6354163G>C	NCBI36
NG_011700.1:g.36686G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.1776G>C	ENSP00000507852.1:p.Val592=
ENST00000683395.1:c.1717G>C
ENST00000684087.1:c.1740G>C	ENSP00000506978.1:p.Val580=
ENST00000506362.2:c.1491G>C	ENSP00000424103.2:p.Val497=
ENST00000673642.1:c.1399G>C	ENSP00000501242.1:n.1399G>C
ENST00000673991.1:c.1776G>C	ENSP00000501033.1:p.Val592=
ENST00000226760.5:c.1740G>C MANE Select	ENSP00000226760.1:p.Val580=
ENST00000503569.5:c.1740G>C	ENSP00000423337.1:p.Val580=
ENST00000507765.1:n.1925G>C
NM_001145853.1:c.1740G>C	NP_001139325.1:p.Val580=
NM_006005.3:c.1740G>C MANE Select	NP_005996.2:p.Val580=
XM_017008586.1:c.1749G>C	XP_016864075.1:p.Val583=