Canonical Allele Identifier: CA383465131

Gene: KCNA5

Linked Data

• MyVariant Identifiers: chr12:g.5154089T>A (hg19) ; chr12:g.5044923T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.5044923T>A , CM000674.2:g.5044923T>A	GRCh38
NC_000012.11:g.5154089T>A , CM000674.1:g.5154089T>A	GRCh37
NC_000012.10:g.5024350T>A	NCBI36
NG_012198.1:g.6005T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252321.5:c.776T>A MANE Select	ENSP00000252321.3:p.Val259Asp
ENST00000252321.4:c.776T>A	ENSP00000252321.3:p.Val259Asp
NM_002234.3:c.776T>A	NP_002225.2:p.Val259Asp
NM_002234.4:c.776T>A MANE Select	NP_002225.2:p.Val259Asp