Canonical Allele Identifier: CA689643436
Gene: KCNA5 HGNC NCBI

Linked Data

dbSNP Id: rs1054827053
gnomAD v3: 12-5044097-G-C
gnomAD v4: 12-5044097-G-C
MyVariant Identifiers: chr12:g.5153263G>C (hg19) chr12:g.5044097G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5044097G>C , CM000674.2:g.5044097G>C GRCh38
NC_000012.11:g.5153263G>C , CM000674.1:g.5153263G>C GRCh37
NC_000012.10:g.5023524G>C NCBI36
NG_012198.1:g.5179G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252321.5:c.-51G>C MANE Select ENSP00000252321.3:n.-51G>C
ENST00000252321.4:c.-51G>C ENSP00000252321.3:n.-51G>C
NM_002234.3:c.-51G>C NP_002225.2:n.-51G>C
NM_002234.4:c.-51G>C MANE Select NP_002225.2:n.-51G>C
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