Canonical Allele Identifier: CA356178771
Gene: WFS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.6304029A>C (hg19) chr4:g.6302302A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302302A>C , CM000666.2:g.6302302A>C GRCh38
NC_000004.11:g.6304029A>C , CM000666.1:g.6304029A>C GRCh37
NC_000004.10:g.6354930A>C NCBI36
NG_011700.1:g.37453A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.2543A>C ENSP00000507852.1:p.Lys848Thr
ENST00000683395.1:c.2484A>C
ENST00000684087.1:c.2507A>C ENSP00000506978.1:p.Lys836Thr
ENST00000506362.2:c.2258A>C ENSP00000424103.2:p.Lys753Thr
ENST00000673991.1:c.2543A>C ENSP00000501033.1:p.Lys848Thr
ENST00000226760.5:c.2507A>C MANE Select ENSP00000226760.1:p.Lys836Thr
ENST00000503569.5:c.2507A>C ENSP00000423337.1:p.Lys836Thr
ENST00000507765.1:n.2692A>C
NM_001145853.1:c.2507A>C NP_001139325.1:p.Lys836Thr
NM_006005.3:c.2507A>C MANE Select NP_005996.2:p.Lys836Thr
XM_017008586.1:c.2516A>C XP_016864075.1:p.Lys839Thr
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