Canonical Allele Identifier: CA438368529

Gene: WFS1

Linked Data

• MyVariant Identifiers: chr4:g.6303628C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301901C>T , CM000666.2:g.6301901C>T	GRCh38
NC_000004.11:g.6303628C>T , CM000666.1:g.6303628C>T	GRCh37
NC_000004.10:g.6354529C>T	NCBI36
NG_011700.1:g.37052C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.2142C>T	ENSP00000507852.1:p.Gly714=
ENST00000683395.1:c.2083C>T
ENST00000684087.1:c.2106C>T	ENSP00000506978.1:p.Gly702=
ENST00000506362.2:c.1857C>T	ENSP00000424103.2:p.Gly619=
ENST00000673642.1:c.1765C>T	ENSP00000501242.1:n.1765C>T
ENST00000673991.1:c.2142C>T	ENSP00000501033.1:p.Gly714=
ENST00000226760.5:c.2106C>T MANE Select	ENSP00000226760.1:p.Gly702=
ENST00000503569.5:c.2106C>T	ENSP00000423337.1:p.Gly702=
ENST00000507765.1:n.2291C>T
NM_001145853.1:c.2106C>T	NP_001139325.1:p.Gly702=
NM_006005.3:c.2106C>T MANE Select	NP_005996.2:p.Gly702=
XM_017008586.1:c.2115C>T	XP_016864075.1:p.Gly705=