Canonical Allele Identifier: CA383461878
Gene: KCNA5 HGNC NCBI

Linked Data

ClinVar Variation Id: 855013
ClinVar RCV Id: RCV001060176
dbSNP Id: rs1862742154
MyVariant Identifiers: chr12:g.5153404G>C (hg19) chr12:g.5044238G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5044238G>C , CM000674.2:g.5044238G>C GRCh38
NC_000012.11:g.5153404G>C , CM000674.1:g.5153404G>C GRCh37
NC_000012.10:g.5023665G>C NCBI36
NG_012198.1:g.5320G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252321.5:c.91G>C MANE Select ENSP00000252321.3:p.Gly31Arg
ENST00000252321.4:c.91G>C ENSP00000252321.3:p.Gly31Arg
NM_002234.3:c.91G>C NP_002225.2:p.Gly31Arg
NM_002234.4:c.91G>C MANE Select NP_002225.2:p.Gly31Arg
Search 100 bp 5'
Search 100 bp 3'