Canonical Allele Identifier: CA29254060

Gene: KCNA3

Linked Data

• dbSNP Id: rs183581761
• gnomAD v2: 1-111215523-T-C
• gnomAD v3: 1-110672901-T-C
• gnomAD v4: 1-110672901-T-C
• MyVariant Identifiers: chr1:g.111215523T>C (hg19) ; chr1:g.110672901T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.110672901T>C , CM000663.2:g.110672901T>C	GRCh38
NC_000001.10:g.111215523T>C , CM000663.1:g.111215523T>C	GRCh37
NC_000001.9:g.111017046T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685980.2:c.*181A>G	ENSP00000513296.1:n.*181A>G
ENST00000697409.1:c.*181A>G	ENSP00000513297.1:n.*181A>G
ENST00000697410.1:c.*181A>G	ENSP00000513298.1:n.*181A>G
ENST00000697411.1:c.1573+336A>G	ENSP00000513299.1:n.1573+336A>G
ENST00000697412.1:c.*181A>G	ENSP00000513300.1:n.*181A>G
ENST00000369769.4:c.*181A>G MANE Select	ENSP00000358784.2:n.*181A>G
ENST00000369769.3:c.*181A>G	ENSP00000358784.2:n.*181A>G
NM_002232.4:c.*181A>G	NP_002223.3:n.*181A>G
NR_109845.1:n.218+336A>G
XR_001738182.1:n.569-13473T>C
XR_001738183.1:n.567-13473T>C
XR_001738184.1:n.573-13473T>C
XR_001738185.1:n.568-13473T>C
XR_001738186.1:n.572-13473T>C
XR_001738187.1:n.570-13473T>C
NM_002232.5:c.*181A>G MANE Select	NP_002223.3:n.*181A>G
NR_109845.2:n.218+336A>G