Canonical Allele Identifier: CA525487494

Gene: KCNA3

Linked Data

• dbSNP Id: rs1333099372
• gnomAD v2: 1-111215378-T-A
• gnomAD v3: 1-110672756-T-A
• gnomAD v4: 1-110672756-T-A
• MyVariant Identifiers: chr1:g.111215378T>A (hg19) ; chr1:g.110672756T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.110672756T>A , CM000663.2:g.110672756T>A	GRCh38
NC_000001.10:g.111215378T>A , CM000663.1:g.111215378T>A	GRCh37
NC_000001.9:g.111016901T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000685980.2:c.*326A>T	ENSP00000513296.1:n.*326A>T
ENST00000697409.1:c.*326A>T	ENSP00000513297.1:n.*326A>T
ENST00000697410.1:c.*326A>T	ENSP00000513298.1:n.*326A>T
ENST00000697411.1:c.1573+481A>T	ENSP00000513299.1:n.1573+481A>T
ENST00000697412.1:c.*326A>T	ENSP00000513300.1:n.*326A>T
ENST00000369769.4:c.*326A>T MANE Select	ENSP00000358784.2:n.*326A>T
ENST00000369769.3:c.*326A>T	ENSP00000358784.2:n.*326A>T
NM_002232.4:c.*326A>T	NP_002223.3:n.*326A>T
NR_109845.1:n.218+481A>T
XR_001738182.1:n.569-13618T>A
XR_001738183.1:n.567-13618T>A
XR_001738184.1:n.573-13618T>A
XR_001738185.1:n.568-13618T>A
XR_001738186.1:n.572-13618T>A
XR_001738187.1:n.570-13618T>A
NM_002232.5:c.*326A>T MANE Select	NP_002223.3:n.*326A>T
NR_109845.2:n.218+481A>T