Canonical Allele Identifier: CA2647068805

Gene: KCNA3

Linked Data

• gnomAD v4: 1-110672891-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.110672891G>A , CM000663.2:g.110672891G>A	GRCh38
NC_000001.10:g.111215513G>A , CM000663.1:g.111215513G>A	GRCh37
NC_000001.9:g.111017036G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685980.2:c.*191C>T	ENSP00000513296.1:n.*191C>T
ENST00000697409.1:c.*191C>T	ENSP00000513297.1:n.*191C>T
ENST00000697410.1:c.*191C>T	ENSP00000513298.1:n.*191C>T
ENST00000697411.1:c.1573+346C>T	ENSP00000513299.1:n.1573+346C>T
ENST00000697412.1:c.*191C>T	ENSP00000513300.1:n.*191C>T
ENST00000369769.4:c.*191C>T MANE Select	ENSP00000358784.2:n.*191C>T
ENST00000369769.3:c.*191C>T	ENSP00000358784.2:n.*191C>T
NM_002232.4:c.*191C>T	NP_002223.3:n.*191C>T
NR_109845.1:n.218+346C>T
XR_001738182.1:n.569-13483G>A
XR_001738183.1:n.567-13483G>A
XR_001738184.1:n.573-13483G>A
XR_001738185.1:n.568-13483G>A
XR_001738186.1:n.572-13483G>A
XR_001738187.1:n.570-13483G>A
NM_002232.5:c.*191C>T MANE Select	NP_002223.3:n.*191C>T
NR_109845.2:n.218+346C>T