Canonical Allele Identifier: CA2840111976

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150950900G>T , CM000669.2:g.150950900G>T	GRCh38
NC_000007.13:g.150647988G>T , CM000669.1:g.150647988G>T	GRCh37
NC_000007.12:g.150278921G>T	NCBI36
NG_008916.1:g.32027C>A , LRG_288:g.32027C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1443+21C>A
ENST00000683359.1:n.290C>A
ENST00000684241.1:n.2978+21C>A
ENST00000262186.10:c.2145+21C>A MANE Select	ENSP00000262186.5:n.2145+21C>A
ENST00000330883.9:c.1125+21C>A	ENSP00000328531.4:n.1125+21C>A
ENST00000262186.9:c.2145+21C>A	ENSP00000262186.5:n.2145+21C>A
ENST00000330883.8:c.1125+21C>A	ENSP00000328531.4:n.1125+21C>A
ENST00000430723.4:c.1797+21C>A	ENSP00000387657.4:n.1797+21C>A
ENST00000461280.1:n.1432+21C>A
ENST00000473610.5:n.1777+21C>A
ENST00000532957.5:n.2368+21C>A
NM_000238.3:c.2145+21C>A , LRG_288t1:c.2145+21C>A	NP_000229.1:n.2145+21C>A
NM_001204798.1:c.1125+21C>A	NP_001191727.1:n.1125+21C>A
NM_172056.2:c.2145+21C>A , LRG_288t2:c.2145+21C>A	NP_742053.1:n.2145+21C>A
NM_172057.2:c.1125+21C>A , LRG_288t3:c.1125+21C>A	NP_742054.1:n.1125+21C>A
XM_011516185.1:c.1845+21C>A	XP_011514487.1:n.1845+21C>A
XM_011516186.1:c.2145+21C>A	XP_011514488.1:n.2145+21C>A
XM_011516185.2:c.1845+21C>A	XP_011514487.1:n.1845+21C>A
XM_011516186.3:c.2145+21C>A	XP_011514488.1:n.2145+21C>A
XM_017012195.1:c.1995+21C>A	XP_016867684.1:n.1995+21C>A
XM_017012196.1:c.1968+21C>A	XP_016867685.1:n.1968+21C>A
NM_000238.4:c.2145+21C>A MANE Select	NP_000229.1:n.2145+21C>A
NM_001204798.2:c.1125+21C>A	NP_001191727.1:n.1125+21C>A
NM_172057.3:c.1125+21C>A	NP_742054.1:n.1125+21C>A