Canonical Allele Identifier: CA2669843575
Gene: WFS1 HGNC NCBI

Linked Data

gnomAD v4: 4-6302569-CGTGTGCAGACTGTG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302571_6302584del , CM000666.2:g.6302571_6302584del GRCh38
NC_000004.11:g.6304298_6304311del , CM000666.1:g.6304298_6304311del GRCh37
NC_000004.10:g.6355199_6355212del NCBI36
NG_011700.1:g.37722_37735del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.*103_*116del ENSP00000507852.1:n.*103_*116del
ENST00000683395.1:c.2753_2766del
ENST00000684087.1:c.*103_*116del ENSP00000506978.1:n.*103_*116del
ENST00000506362.2:c.*103_*116del ENSP00000424103.2:n.*103_*116del
ENST00000673991.1:c.*103_*116del ENSP00000501033.1:n.*103_*116del
ENST00000226760.5:c.*103_*116del MANE Select ENSP00000226760.1:n.*103_*116del
ENST00000503569.5:c.*103_*116del ENSP00000423337.1:n.*103_*116del
ENST00000507765.1:n.2961_2974del
NM_001145853.1:c.*103_*116del NP_001139325.1:n.*103_*116del
NM_006005.3:c.*103_*116del MANE Select NP_005996.2:n.*103_*116del
XM_017008586.1:c.*103_*116del XP_016864075.1:n.*103_*116del
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