Canonical Allele Identifier: CA356177565
Gene: WFS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.6303555G>T (hg19) chr4:g.6301828G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6301828G>T , CM000666.2:g.6301828G>T GRCh38
NC_000004.11:g.6303555G>T , CM000666.1:g.6303555G>T GRCh37
NC_000004.10:g.6354456G>T NCBI36
NG_011700.1:g.36979G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.2069G>T ENSP00000507852.1:p.Trp690Leu
ENST00000683395.1:c.2010G>T
ENST00000684087.1:c.2033G>T ENSP00000506978.1:p.Trp678Leu
ENST00000506362.2:c.1784G>T ENSP00000424103.2:p.Trp595Leu
ENST00000673642.1:c.1692G>T ENSP00000501242.1:n.1692G>T
ENST00000673991.1:c.2069G>T ENSP00000501033.1:p.Trp690Leu
ENST00000226760.5:c.2033G>T MANE Select ENSP00000226760.1:p.Trp678Leu
ENST00000503569.5:c.2033G>T ENSP00000423337.1:p.Trp678Leu
ENST00000507765.1:n.2218G>T
NM_001145853.1:c.2033G>T NP_001139325.1:p.Trp678Leu
NM_006005.3:c.2033G>T MANE Select NP_005996.2:p.Trp678Leu
XM_017008586.1:c.2042G>T XP_016864075.1:p.Trp681Leu
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