Canonical Allele Identifier: CA356178342

Gene: WFS1

Linked Data

• ClinVar Variation Id: 1458820
• ClinVar RCV Id: RCV001958688
• dbSNP Id: rs534067035
• MyVariant Identifiers: chr4:g.6303833G>C (hg19) ; chr4:g.6302106G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302106G>C , CM000666.2:g.6302106G>C	GRCh38
NC_000004.11:g.6303833G>C , CM000666.1:g.6303833G>C	GRCh37
NC_000004.10:g.6354734G>C	NCBI36
NG_011700.1:g.37257G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.2347G>C	ENSP00000507852.1:p.Asp783His
ENST00000683395.1:c.2288G>C
ENST00000684087.1:c.2311G>C	ENSP00000506978.1:p.Asp771His
ENST00000506362.2:c.2062G>C	ENSP00000424103.2:p.Asp688His
ENST00000673642.1:c.1970G>C	ENSP00000501242.1:n.1970G>C
ENST00000673991.1:c.2347G>C	ENSP00000501033.1:p.Asp783His
ENST00000226760.5:c.2311G>C MANE Select	ENSP00000226760.1:p.Asp771His
ENST00000503569.5:c.2311G>C	ENSP00000423337.1:p.Asp771His
ENST00000507765.1:n.2496G>C
NM_001145853.1:c.2311G>C	NP_001139325.1:p.Asp771His
NM_006005.3:c.2311G>C MANE Select	NP_005996.2:p.Asp771His
XM_017008586.1:c.2320G>C	XP_016864075.1:p.Asp774His