Canonical Allele Identifier: CA28809737

Gene: KCNA2

Linked Data

• dbSNP Id: rs188801376
• gnomAD v2: 1-111148083-C-T
• gnomAD v3: 1-110605461-C-T
• gnomAD v4: 1-110605461-C-T
• MyVariant Identifiers: chr1:g.111148083C>T (hg19) ; chr1:g.110605461C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.110605461C>T , CM000663.2:g.110605461C>T	GRCh38
NC_000001.10:g.111148083C>T , CM000663.1:g.111148083C>T	GRCh37
NC_000001.9:g.110949606C>T	NCBI36
NG_027997.2:g.31014G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000316361.10:c.-234G>A MANE Select	ENSP00000314520.4:n.-234G>A
ENST00000485317.6:c.-234G>A	ENSP00000433109.1:n.-234G>A
ENST00000525120.2:n.291G>A
ENST00000638477.2:c.-157G>A	ENSP00000491354.1:n.-157G>A
ENST00000638532.1:c.-234G>A	ENSP00000491613.1:n.-234G>A
ENST00000638616.2:c.-234G>A	ENSP00000491977.1:n.-234G>A
ENST00000639048.2:c.-157G>A	ENSP00000491627.1:n.-157G>A
ENST00000639233.2:c.-117G>A	ENSP00000492716.1:n.-117G>A
ENST00000640680.1:n.389G>A
ENST00000640774.2:c.-157G>A	ENSP00000492008.1:n.-157G>A
ENST00000640956.1:c.-118G>A	ENSP00000491647.1:n.-118G>A
ENST00000675391.1:c.-444G>A	ENSP00000502642.1:n.-444G>A
ENST00000316361.8:c.-234G>A	ENSP00000314520.4:n.-234G>A
ENST00000369770.7:c.-234G>A	ENSP00000358785.3:n.-234G>A
ENST00000485317.5:c.-234G>A	ENSP00000433109.1:n.-234G>A
ENST00000525120.1:n.399G>A
ENST00000633222.1:c.-234G>A	ENSP00000487785.1:n.-234G>A
NM_001204269.1:c.-234G>A	NP_001191198.1:n.-234G>A
NM_004974.3:c.-234G>A	NP_004965.1:n.-234G>A
XM_011541396.1:c.-234G>A	XP_011539698.1:n.-234G>A
XM_011541397.1:c.-234G>A	XP_011539699.1:n.-234G>A
XM_011541398.1:c.-234G>A	XP_011539700.1:n.-234G>A
XM_011541399.1:c.-234G>A	XP_011539701.1:n.-234G>A
XM_011541400.1:c.-234G>A	XP_011539702.1:n.-234G>A
XM_011541396.2:c.-234G>A	XP_011539698.1:n.-234G>A
XM_011541397.2:c.-234G>A	XP_011539699.1:n.-234G>A
XM_011541398.2:c.-234G>A	XP_011539700.1:n.-234G>A
XM_011541399.2:c.-234G>A	XP_011539701.1:n.-234G>A
XM_011541400.2:c.-234G>A	XP_011539702.1:n.-234G>A
XM_017001213.1:c.-234G>A	XP_016856702.1:n.-234G>A
NM_004974.4:c.-234G>A MANE Select	NP_004965.1:n.-234G>A
NM_001204269.2:c.-234G>A	NP_001191198.1:n.-234G>A