Canonical Allele Identifier: CA383466443
Gene: KCNA5 HGNC NCBI

Linked Data

gnomAD v4: 12-5045563-G-T
MyVariant Identifiers: chr12:g.5154729G>T (hg19) chr12:g.5045563G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5045563G>T , CM000674.2:g.5045563G>T GRCh38
NC_000012.11:g.5154729G>T , CM000674.1:g.5154729G>T GRCh37
NC_000012.10:g.5024990G>T NCBI36
NG_012198.1:g.6645G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252321.5:c.1416G>T MANE Select ENSP00000252321.3:p.Trp472Cys
ENST00000252321.4:c.1416G>T ENSP00000252321.3:p.Trp472Cys
NM_002234.3:c.1416G>T NP_002225.2:p.Trp472Cys
NM_002234.4:c.1416G>T MANE Select NP_002225.2:p.Trp472Cys
Search 100 bp 5'
Search 100 bp 3'