Canonical Allele Identifier: CA2647068620
Gene: KCNA3 HGNC NCBI

Linked Data

gnomAD v4: 1-110672783-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.110672783C>T , CM000663.2:g.110672783C>T GRCh38
NC_000001.10:g.111215405C>T , CM000663.1:g.111215405C>T GRCh37
NC_000001.9:g.111016928C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000685980.2:c.*299G>A ENSP00000513296.1:n.*299G>A
ENST00000697409.1:c.*299G>A ENSP00000513297.1:n.*299G>A
ENST00000697410.1:c.*299G>A ENSP00000513298.1:n.*299G>A
ENST00000697411.1:c.1573+454G>A ENSP00000513299.1:n.1573+454G>A
ENST00000697412.1:c.*299G>A ENSP00000513300.1:n.*299G>A
ENST00000369769.4:c.*299G>A MANE Select ENSP00000358784.2:n.*299G>A
ENST00000369769.3:c.*299G>A ENSP00000358784.2:n.*299G>A
NM_002232.4:c.*299G>A NP_002223.3:n.*299G>A
NR_109845.1:n.218+454G>A
XR_001738182.1:n.569-13591C>T
XR_001738183.1:n.567-13591C>T
XR_001738184.1:n.573-13591C>T
XR_001738185.1:n.568-13591C>T
XR_001738186.1:n.572-13591C>T
XR_001738187.1:n.570-13591C>T
NM_002232.5:c.*299G>A MANE Select NP_002223.3:n.*299G>A
NR_109845.2:n.218+454G>A
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