Canonical Allele Identifier: CA438211048

Gene: WFS1

Linked Data

• MyVariant Identifiers: chr4:g.6293660A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291933A>G , CM000666.2:g.6291933A>G	GRCh38
NC_000004.11:g.6293660A>G , CM000666.1:g.6293660A>G	GRCh37
NC_000004.10:g.6344561A>G	NCBI36
NG_011700.1:g.27084A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.648A>G	ENSP00000507852.1:p.Pro216=
ENST00000683395.1:c.625A>G
ENST00000684087.1:c.648A>G	ENSP00000506978.1:p.Pro216=
ENST00000506362.2:c.399A>G	ENSP00000424103.2:p.Pro133=
ENST00000673642.1:c.447A>G	ENSP00000501242.1:p.Pro149=
ENST00000673991.1:c.648A>G	ENSP00000501033.1:p.Pro216=
ENST00000226760.5:c.648A>G MANE Select	ENSP00000226760.1:p.Pro216=
ENST00000503569.5:c.648A>G	ENSP00000423337.1:p.Pro216=
ENST00000506362.1:c.245A>G
ENST00000507765.1:n.833A>G
NM_001145853.1:c.648A>G	NP_001139325.1:p.Pro216=
NM_006005.3:c.648A>G MANE Select	NP_005996.2:p.Pro216=
XM_017008586.1:c.657A>G	XP_016864075.1:p.Pro219=