Canonical Allele Identifier: CA2745030276

Gene: KCNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.110672929A>C , CM000663.2:g.110672929A>C	GRCh38
NC_000001.10:g.111215551A>C , CM000663.1:g.111215551A>C	GRCh37
NC_000001.9:g.111017074A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685980.2:c.*153T>G	ENSP00000513296.1:n.*153T>G
ENST00000697409.1:c.*153T>G	ENSP00000513297.1:n.*153T>G
ENST00000697410.1:c.*153T>G	ENSP00000513298.1:n.*153T>G
ENST00000697411.1:c.1573+308T>G	ENSP00000513299.1:n.1573+308T>G
ENST00000697412.1:c.*153T>G	ENSP00000513300.1:n.*153T>G
ENST00000369769.4:c.*153T>G MANE Select	ENSP00000358784.2:n.*153T>G
ENST00000369769.3:c.*153T>G	ENSP00000358784.2:n.*153T>G
NM_002232.4:c.*153T>G	NP_002223.3:n.*153T>G
NR_109845.1:n.218+308T>G
XR_001738182.1:n.569-13445A>C
XR_001738183.1:n.567-13445A>C
XR_001738184.1:n.573-13445A>C
XR_001738185.1:n.568-13445A>C
XR_001738186.1:n.572-13445A>C
XR_001738187.1:n.570-13445A>C
NM_002232.5:c.*153T>G MANE Select	NP_002223.3:n.*153T>G
NR_109845.2:n.218+308T>G