Canonical Allele Identifier: CA6399527
Gene: KCNA5 HGNC NCBI

Linked Data

dbSNP Id: rs775893669
ExAC: 12:5153296 G / GC
gnomAD v2: 12-5153296-G-GC
gnomAD v4: 12-5044130-G-GC
MyVariant Identifiers: chr12:g.5153296_5153297insC (hg19) chr12:g.5044130_5044131insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5044133dup , CM000674.2:g.5044133dup GRCh38
NC_000012.11:g.5153299dup , CM000674.1:g.5153299dup GRCh37
NC_000012.10:g.5023560dup NCBI36
NG_012198.1:g.5215dup

Transcript Alleles

HGVS Amino-acid change
ENST00000252321.5:c.-15dup MANE Select ENSP00000252321.3:n.-15dup
ENST00000252321.4:c.-15dup ENSP00000252321.3:n.-15dup
NM_002234.3:c.-15dup NP_002225.2:n.-15dup
NM_002234.4:c.-15dup MANE Select NP_002225.2:n.-15dup
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Search 100 bp 3'