Canonical Allele Identifier: CA356177132

Gene: WFS1

Linked Data

• MyVariant Identifiers: chr4:g.6303459T>C (hg19) ; chr4:g.6301732T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301732T>C , CM000666.2:g.6301732T>C	GRCh38
NC_000004.11:g.6303459T>C , CM000666.1:g.6303459T>C	GRCh37
NC_000004.10:g.6354360T>C	NCBI36
NG_011700.1:g.36883T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1973T>C	ENSP00000507852.1:p.Phe658Ser
ENST00000683395.1:c.1914T>C
ENST00000684087.1:c.1937T>C	ENSP00000506978.1:p.Phe646Ser
ENST00000506362.2:c.1688T>C	ENSP00000424103.2:p.Phe563Ser
ENST00000673642.1:c.1596T>C	ENSP00000501242.1:n.1596T>C
ENST00000673991.1:c.1973T>C	ENSP00000501033.1:p.Phe658Ser
ENST00000226760.5:c.1937T>C MANE Select	ENSP00000226760.1:p.Phe646Ser
ENST00000503569.5:c.1937T>C	ENSP00000423337.1:p.Phe646Ser
ENST00000507765.1:n.2122T>C
NM_001145853.1:c.1937T>C	NP_001139325.1:p.Phe646Ser
NM_006005.3:c.1937T>C MANE Select	NP_005996.2:p.Phe646Ser
XM_017008586.1:c.1946T>C	XP_016864075.1:p.Phe649Ser