Canonical Allele Identifier: CA689643419
Gene: KCNA5 HGNC NCBI

Linked Data

dbSNP Id: rs1322199011
MyVariant Identifiers: chr12:g.5153245_5153246insCGCGG (hg19) chr12:g.5044079_5044080insCGCGG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5044080_5044084dup , CM000674.2:g.5044080_5044084dup GRCh38
NC_000012.11:g.5153246_5153250dup , CM000674.1:g.5153246_5153250dup GRCh37
NC_000012.10:g.5023507_5023511dup NCBI36
NG_012198.1:g.5162_5166dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000252321.5:c.-68_-64dup MANE Select ENSP00000252321.3:n.-68_-64dup
ENST00000252321.4:c.-68_-64dup ENSP00000252321.3:n.-68_-64dup
NM_002234.3:c.-68_-64dup NP_002225.2:n.-68_-64dup
NM_002234.4:c.-68_-64dup MANE Select NP_002225.2:n.-68_-64dup
Search 100 bp 5'
Search 100 bp 3'