Canonical Allele Identifier: CA91794587

Gene: WFS1

Linked Data

• dbSNP Id: rs1055820069
• MyVariant Identifiers: chr4:g.6293169G>C (hg19) ; chr4:g.6291442G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291442G>C , CM000666.2:g.6291442G>C	GRCh38
NC_000004.11:g.6293169G>C , CM000666.1:g.6293169G>C	GRCh37
NC_000004.10:g.6344070G>C	NCBI36
NG_011700.1:g.26593G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.631+75G>C	ENSP00000507852.1:n.631+75G>C
ENST00000683395.1:c.608+88G>C
ENST00000684087.1:c.631+75G>C	ENSP00000506978.1:n.631+75G>C
ENST00000684700.1:c.*1G>C	ENSP00000507806.1:n.*1G>C
ENST00000506362.2:c.382+75G>C	ENSP00000424103.2:n.382+75G>C
ENST00000673642.1:c.430+75G>C	ENSP00000501242.1:n.430+75G>C
ENST00000673991.1:c.631+75G>C	ENSP00000501033.1:n.631+75G>C
ENST00000226760.5:c.631+75G>C MANE Select	ENSP00000226760.1:n.631+75G>C
ENST00000503569.5:c.631+75G>C	ENSP00000423337.1:n.631+75G>C
ENST00000506362.1:c.228+75G>C
ENST00000507765.1:n.816+75G>C
NM_001145853.1:c.631+75G>C	NP_001139325.1:n.631+75G>C
NM_006005.3:c.631+75G>C MANE Select	NP_005996.2:n.631+75G>C
XM_017008586.1:c.640+75G>C	XP_016864075.1:n.640+75G>C