Canonical Allele Identifier: CA356179157
Gene: WFS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302329T>A , CM000666.2:g.6302329T>A GRCh38
NC_000004.11:g.6304056T>A , CM000666.1:g.6304056T>A GRCh37
NC_000004.10:g.6354957T>A NCBI36
NG_011700.1:g.37480T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.2570T>A ENSP00000507852.1:p.Ile857Asn
ENST00000683395.1:c.2511T>A
ENST00000684087.1:c.2534T>A ENSP00000506978.1:p.Ile845Asn
ENST00000506362.2:c.2285T>A ENSP00000424103.2:p.Ile762Asn
ENST00000673991.1:c.2570T>A ENSP00000501033.1:p.Ile857Asn
ENST00000226760.5:c.2534T>A MANE Select ENSP00000226760.1:p.Ile845Asn
ENST00000503569.5:c.2534T>A ENSP00000423337.1:p.Ile845Asn
ENST00000507765.1:n.2719T>A
NM_001145853.1:c.2534T>A NP_001139325.1:p.Ile845Asn
NM_006005.3:c.2534T>A MANE Select NP_005996.2:p.Ile845Asn
XM_017008586.1:c.2543T>A XP_016864075.1:p.Ile848Asn