Canonical Allele Identifier: CA383467126
Gene: KCNA5 HGNC NCBI

Linked Data

gnomAD v4: 12-5045891-C-T
MyVariant Identifiers: chr12:g.5155057C>T (hg19) chr12:g.5045891C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5045891C>T , CM000674.2:g.5045891C>T GRCh38
NC_000012.11:g.5155057C>T , CM000674.1:g.5155057C>T GRCh37
NC_000012.10:g.5025318C>T NCBI36
NG_012198.1:g.6973C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252321.5:c.1744C>T MANE Select ENSP00000252321.3:p.Pro582Ser
ENST00000252321.4:c.1744C>T ENSP00000252321.3:p.Pro582Ser
NM_002234.3:c.1744C>T NP_002225.2:p.Pro582Ser
NM_002234.4:c.1744C>T MANE Select NP_002225.2:p.Pro582Ser
Search 100 bp 5'
Search 100 bp 3'