Canonical Allele Identifier: CA383465408
Gene: KCNA5 HGNC NCBI

Linked Data

dbSNP Id: rs1463542784
gnomAD v2: 12-5154229-C-G
gnomAD v4: 12-5045063-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5045063C>G , CM000674.2:g.5045063C>G GRCh38
NC_000012.11:g.5154229C>G , CM000674.1:g.5154229C>G GRCh37
NC_000012.10:g.5024490C>G NCBI36
NG_012198.1:g.6145C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252321.5:c.916C>G MANE Select ENSP00000252321.3:p.Pro306Ala
ENST00000252321.4:c.916C>G ENSP00000252321.3:p.Pro306Ala
NM_002234.3:c.916C>G NP_002225.2:p.Pro306Ala
NM_002234.4:c.916C>G MANE Select NP_002225.2:p.Pro306Ala