Canonical Allele Identifier: CA2647068602

Gene: KCNA3

Linked Data

• gnomAD v4: 1-110672752-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.110672752G>T , CM000663.2:g.110672752G>T	GRCh38
NC_000001.10:g.111215374G>T , CM000663.1:g.111215374G>T	GRCh37
NC_000001.9:g.111016897G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000685980.2:c.*330C>A	ENSP00000513296.1:n.*330C>A
ENST00000697409.1:c.*330C>A	ENSP00000513297.1:n.*330C>A
ENST00000697410.1:c.*330C>A	ENSP00000513298.1:n.*330C>A
ENST00000697411.1:c.1573+485C>A	ENSP00000513299.1:n.1573+485C>A
ENST00000697412.1:c.*330C>A	ENSP00000513300.1:n.*330C>A
ENST00000369769.4:c.*330C>A MANE Select	ENSP00000358784.2:n.*330C>A
ENST00000369769.3:c.*330C>A	ENSP00000358784.2:n.*330C>A
NM_002232.4:c.*330C>A	NP_002223.3:n.*330C>A
NR_109845.1:n.218+485C>A
XR_001738182.1:n.569-13622G>T
XR_001738183.1:n.567-13622G>T
XR_001738184.1:n.573-13622G>T
XR_001738185.1:n.568-13622G>T
XR_001738186.1:n.572-13622G>T
XR_001738187.1:n.570-13622G>T
NM_002232.5:c.*330C>A MANE Select	NP_002223.3:n.*330C>A
NR_109845.2:n.218+485C>A