Canonical Allele Identifier: CA356179243

Gene: WFS1

Linked Data

• MyVariant Identifiers: chr4:g.6304085T>G (hg19) ; chr4:g.6302358T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302358T>G , CM000666.2:g.6302358T>G	GRCh38
NC_000004.11:g.6304085T>G , CM000666.1:g.6304085T>G	GRCh37
NC_000004.10:g.6354986T>G	NCBI36
NG_011700.1:g.37509T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.2599T>G	ENSP00000507852.1:p.Ser867Ala
ENST00000683395.1:c.2540T>G
ENST00000684087.1:c.2563T>G	ENSP00000506978.1:p.Ser855Ala
ENST00000506362.2:c.2314T>G	ENSP00000424103.2:p.Ser772Ala
ENST00000673991.1:c.2599T>G	ENSP00000501033.1:p.Ser867Ala
ENST00000226760.5:c.2563T>G MANE Select	ENSP00000226760.1:p.Ser855Ala
ENST00000503569.5:c.2563T>G	ENSP00000423337.1:p.Ser855Ala
ENST00000507765.1:n.2748T>G
NM_001145853.1:c.2563T>G	NP_001139325.1:p.Ser855Ala
NM_006005.3:c.2563T>G MANE Select	NP_005996.2:p.Ser855Ala
XM_017008586.1:c.2572T>G	XP_016864075.1:p.Ser858Ala