Canonical Allele Identifier: CA356179282
Gene: WFS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.6304098G>C (hg19) chr4:g.6302371G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302371G>C , CM000666.2:g.6302371G>C GRCh38
NC_000004.11:g.6304098G>C , CM000666.1:g.6304098G>C GRCh37
NC_000004.10:g.6354999G>C NCBI36
NG_011700.1:g.37522G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.2612G>C ENSP00000507852.1:p.Arg871Pro
ENST00000683395.1:c.2553G>C
ENST00000684087.1:c.2576G>C ENSP00000506978.1:p.Arg859Pro
ENST00000506362.2:c.2327G>C ENSP00000424103.2:p.Arg776Pro
ENST00000673991.1:c.2612G>C ENSP00000501033.1:p.Arg871Pro
ENST00000226760.5:c.2576G>C MANE Select ENSP00000226760.1:p.Arg859Pro
ENST00000503569.5:c.2576G>C ENSP00000423337.1:p.Arg859Pro
ENST00000507765.1:n.2761G>C
NM_001145853.1:c.2576G>C NP_001139325.1:p.Arg859Pro
NM_006005.3:c.2576G>C MANE Select NP_005996.2:p.Arg859Pro
XM_017008586.1:c.2585G>C XP_016864075.1:p.Arg862Pro
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