Canonical Allele Identifier: CA2745030267

Gene: KCNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.110672771T>C , CM000663.2:g.110672771T>C	GRCh38
NC_000001.10:g.111215393T>C , CM000663.1:g.111215393T>C	GRCh37
NC_000001.9:g.111016916T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685980.2:c.*311A>G	ENSP00000513296.1:n.*311A>G
ENST00000697409.1:c.*311A>G	ENSP00000513297.1:n.*311A>G
ENST00000697410.1:c.*311A>G	ENSP00000513298.1:n.*311A>G
ENST00000697411.1:c.1573+466A>G	ENSP00000513299.1:n.1573+466A>G
ENST00000697412.1:c.*311A>G	ENSP00000513300.1:n.*311A>G
ENST00000369769.4:c.*311A>G MANE Select	ENSP00000358784.2:n.*311A>G
ENST00000369769.3:c.*311A>G	ENSP00000358784.2:n.*311A>G
NM_002232.4:c.*311A>G	NP_002223.3:n.*311A>G
NR_109845.1:n.218+466A>G
XR_001738182.1:n.569-13603T>C
XR_001738183.1:n.567-13603T>C
XR_001738184.1:n.573-13603T>C
XR_001738185.1:n.568-13603T>C
XR_001738186.1:n.572-13603T>C
XR_001738187.1:n.570-13603T>C
NM_002232.5:c.*311A>G MANE Select	NP_002223.3:n.*311A>G
NR_109845.2:n.218+466A>G