Canonical Allele Identifier: CA603072771
Gene: KCNA5 HGNC NCBI

Linked Data

dbSNP Id: rs1186532195
gnomAD v2: 12-5155191-G-A
MyVariant Identifiers: chr12:g.5155191G>A (hg19) chr12:g.5046025G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5046025G>A , CM000674.2:g.5046025G>A GRCh38
NC_000012.11:g.5155191G>A , CM000674.1:g.5155191G>A GRCh37
NC_000012.10:g.5025452G>A NCBI36
NG_012198.1:g.7107G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252321.5:c.*36G>A MANE Select ENSP00000252321.3:n.*36G>A
ENST00000252321.4:c.*36G>A ENSP00000252321.3:n.*36G>A
NM_002234.3:c.*36G>A NP_002225.2:n.*36G>A
NM_002234.4:c.*36G>A MANE Select NP_002225.2:n.*36G>A
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Search 100 bp 3'