Canonical Allele Identifier: CA356171904

Gene: WFS1

Linked Data

• MyVariant Identifiers: chr4:g.6292959C>G (hg19) ; chr4:g.6291232C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291232C>G , CM000666.2:g.6291232C>G	GRCh38
NC_000004.11:g.6292959C>G , CM000666.1:g.6292959C>G	GRCh37
NC_000004.10:g.6343860C>G	NCBI36
NG_011700.1:g.26383C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.496C>G	ENSP00000507852.1:p.Leu166Val
ENST00000683395.1:c.486C>G
ENST00000684087.1:c.496C>G	ENSP00000506978.1:p.Leu166Val
ENST00000684700.1:c.496C>G	ENSP00000507806.1:p.Leu166Val
ENST00000506362.2:c.247C>G	ENSP00000424103.2:p.Leu83Val
ENST00000673642.1:c.295C>G	ENSP00000501242.1:p.Leu99Val
ENST00000673991.1:c.496C>G	ENSP00000501033.1:p.Leu166Val
ENST00000674051.1:c.370C>G	ENSP00000501083.1:p.Leu124Val
ENST00000226760.5:c.496C>G MANE Select	ENSP00000226760.1:p.Leu166Val
ENST00000503569.5:c.496C>G	ENSP00000423337.1:p.Leu166Val
ENST00000506362.1:c.93C>G
ENST00000507765.1:n.681C>G
NM_001145853.1:c.496C>G	NP_001139325.1:p.Leu166Val
NM_006005.3:c.496C>G MANE Select	NP_005996.2:p.Leu166Val
XM_017008586.1:c.505C>G	XP_016864075.1:p.Leu169Val