Canonical Allele Identifier: CA2617209611
Gene: KCNA5 HGNC NCBI

Linked Data

gnomAD v4: 12-5043937-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5043937C>A , CM000674.2:g.5043937C>A GRCh38
NC_000012.11:g.5153103C>A , CM000674.1:g.5153103C>A GRCh37
NC_000012.10:g.5023364C>A NCBI36
NG_012198.1:g.5019C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252321.5:c.-211C>A MANE Select ENSP00000252321.3:n.-211C>A
NM_002234.3:c.-211C>A NP_002225.2:n.-211C>A
NM_002234.4:c.-211C>A MANE Select NP_002225.2:n.-211C>A
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