Canonical Allele Identifier: CA1188605066

Gene: KCNA3

Linked Data

• dbSNP Id: rs1651933562
• gnomAD v4: 1-110672775-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.110672775A>G , CM000663.2:g.110672775A>G	GRCh38
NC_000001.10:g.111215397A>G , CM000663.1:g.111215397A>G	GRCh37
NC_000001.9:g.111016920A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000685980.2:c.*307T>C	ENSP00000513296.1:n.*307T>C
ENST00000697409.1:c.*307T>C	ENSP00000513297.1:n.*307T>C
ENST00000697410.1:c.*307T>C	ENSP00000513298.1:n.*307T>C
ENST00000697411.1:c.1573+462T>C	ENSP00000513299.1:n.1573+462T>C
ENST00000697412.1:c.*307T>C	ENSP00000513300.1:n.*307T>C
ENST00000369769.4:c.*307T>C MANE Select	ENSP00000358784.2:n.*307T>C
ENST00000369769.3:c.*307T>C	ENSP00000358784.2:n.*307T>C
NM_002232.4:c.*307T>C	NP_002223.3:n.*307T>C
NR_109845.1:n.218+462T>C
XR_001738182.1:n.569-13599A>G
XR_001738183.1:n.567-13599A>G
XR_001738184.1:n.573-13599A>G
XR_001738185.1:n.568-13599A>G
XR_001738186.1:n.572-13599A>G
XR_001738187.1:n.570-13599A>G
NM_002232.5:c.*307T>C MANE Select	NP_002223.3:n.*307T>C
NR_109845.2:n.218+462T>C