Canonical Allele Identifier: CA885455130
Gene: KCNA2 HGNC NCBI

Linked Data

dbSNP Id: rs1190819368

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.110605476C>T , CM000663.2:g.110605476C>T GRCh38
NC_000001.10:g.111148098C>T , CM000663.1:g.111148098C>T GRCh37
NC_000001.9:g.110949621C>T NCBI36
NG_027997.2:g.30999G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000316361.10:c.-249G>A MANE Select ENSP00000314520.4:n.-249G>A
ENST00000485317.6:c.-249G>A ENSP00000433109.1:n.-249G>A
ENST00000525120.2:n.276G>A
ENST00000638477.2:c.-172G>A ENSP00000491354.1:n.-172G>A
ENST00000638532.1:c.-249G>A ENSP00000491613.1:n.-249G>A
ENST00000638616.2:c.-249G>A ENSP00000491977.1:n.-249G>A
ENST00000639048.2:c.-172G>A ENSP00000491627.1:n.-172G>A
ENST00000639233.2:c.-132G>A ENSP00000492716.1:n.-132G>A
ENST00000640680.1:n.374G>A
ENST00000640774.2:c.-172G>A ENSP00000492008.1:n.-172G>A
ENST00000640956.1:c.-133G>A ENSP00000491647.1:n.-133G>A
ENST00000675391.1:c.-459G>A ENSP00000502642.1:n.-459G>A
ENST00000316361.8:c.-249G>A ENSP00000314520.4:n.-249G>A
ENST00000369770.7:c.-249G>A ENSP00000358785.3:n.-249G>A
ENST00000485317.5:c.-249G>A ENSP00000433109.1:n.-249G>A
ENST00000525120.1:n.384G>A
ENST00000633222.1:c.-249G>A ENSP00000487785.1:n.-249G>A
NM_001204269.1:c.-249G>A NP_001191198.1:n.-249G>A
NM_004974.3:c.-249G>A NP_004965.1:n.-249G>A
XM_011541396.1:c.-249G>A XP_011539698.1:n.-249G>A
XM_011541397.1:c.-249G>A XP_011539699.1:n.-249G>A
XM_011541398.1:c.-249G>A XP_011539700.1:n.-249G>A
XM_011541399.1:c.-249G>A XP_011539701.1:n.-249G>A
XM_011541400.1:c.-249G>A XP_011539702.1:n.-249G>A
XM_011541396.2:c.-249G>A XP_011539698.1:n.-249G>A
XM_011541397.2:c.-249G>A XP_011539699.1:n.-249G>A
XM_011541398.2:c.-249G>A XP_011539700.1:n.-249G>A
XM_011541399.2:c.-249G>A XP_011539701.1:n.-249G>A
XM_011541400.2:c.-249G>A XP_011539702.1:n.-249G>A
XM_017001213.1:c.-249G>A XP_016856702.1:n.-249G>A
NM_004974.4:c.-249G>A MANE Select NP_004965.1:n.-249G>A
NM_001204269.2:c.-249G>A NP_001191198.1:n.-249G>A