Canonical Allele Identifier: CA2669844057
Gene: WFS1 HGNC NCBI

Linked Data

gnomAD v4: 4-6303046-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6303046A>G , CM000666.2:g.6303046A>G GRCh38
NC_000004.11:g.6304773A>G , CM000666.1:g.6304773A>G GRCh37
NC_000004.10:g.6355674A>G NCBI36
NG_011700.1:g.38197A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.*578A>G ENSP00000507852.1:n.*578A>G
ENST00000683395.1:c.3228A>G
ENST00000684087.1:c.*578A>G ENSP00000506978.1:n.*578A>G
ENST00000673991.1:c.*578A>G ENSP00000501033.1:n.*578A>G
ENST00000226760.5:c.*578A>G MANE Select ENSP00000226760.1:n.*578A>G
ENST00000507765.1:n.3436A>G
NM_001145853.1:c.*578A>G NP_001139325.1:n.*578A>G
NM_006005.3:c.*578A>G MANE Select NP_005996.2:n.*578A>G
XM_017008586.1:c.*578A>G XP_016864075.1:n.*578A>G
XR_001741566.2:n.1899T>C
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