Canonical Allele Identifier: CA383466589
Gene: KCNA5 HGNC NCBI

Linked Data

dbSNP Id: rs760979131
MyVariant Identifiers: chr12:g.5154796A>T (hg19) chr12:g.5045630A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5045630A>T , CM000674.2:g.5045630A>T GRCh38
NC_000012.11:g.5154796A>T , CM000674.1:g.5154796A>T GRCh37
NC_000012.10:g.5025057A>T NCBI36
NG_012198.1:g.6712A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252321.5:c.1483A>T MANE Select ENSP00000252321.3:p.Ile495Phe
ENST00000252321.4:c.1483A>T ENSP00000252321.3:p.Ile495Phe
NM_002234.3:c.1483A>T NP_002225.2:p.Ile495Phe
NM_002234.4:c.1483A>T MANE Select NP_002225.2:p.Ile495Phe
Search 100 bp 5'
Search 100 bp 3'