Canonical Allele Identifier: CA2647068609

Gene: KCNA3

Linked Data

• gnomAD v4: 1-110672770-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.110672770C>T , CM000663.2:g.110672770C>T	GRCh38
NC_000001.10:g.111215392C>T , CM000663.1:g.111215392C>T	GRCh37
NC_000001.9:g.111016915C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000685980.2:c.*312G>A	ENSP00000513296.1:n.*312G>A
ENST00000697409.1:c.*312G>A	ENSP00000513297.1:n.*312G>A
ENST00000697410.1:c.*312G>A	ENSP00000513298.1:n.*312G>A
ENST00000697411.1:c.1573+467G>A	ENSP00000513299.1:n.1573+467G>A
ENST00000697412.1:c.*312G>A	ENSP00000513300.1:n.*312G>A
ENST00000369769.4:c.*312G>A MANE Select	ENSP00000358784.2:n.*312G>A
ENST00000369769.3:c.*312G>A	ENSP00000358784.2:n.*312G>A
NM_002232.4:c.*312G>A	NP_002223.3:n.*312G>A
NR_109845.1:n.218+467G>A
XR_001738182.1:n.569-13604C>T
XR_001738183.1:n.567-13604C>T
XR_001738184.1:n.573-13604C>T
XR_001738185.1:n.568-13604C>T
XR_001738186.1:n.572-13604C>T
XR_001738187.1:n.570-13604C>T
NM_002232.5:c.*312G>A MANE Select	NP_002223.3:n.*312G>A
NR_109845.2:n.218+467G>A