Canonical Allele Identifier: CA004841

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951812C>T , CM000669.2:g.150951812C>T	GRCh38
NC_000007.13:g.150648900C>T , CM000669.1:g.150648900C>T	GRCh37
NC_000007.12:g.150279833C>T	NCBI36
NG_008916.1:g.31115G>A , LRG_288:g.31115G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.879G>A
ENST00000684116.1:n.474G>A
ENST00000684241.1:n.2414G>A
ENST00000262186.10:c.1581G>A MANE Select	ENSP00000262186.5:p.Ala527=
ENST00000330883.9:c.561G>A	ENSP00000328531.4:p.Ala187=
ENST00000262186.9:c.1581G>A	ENSP00000262186.5:p.Ala527=
ENST00000330883.8:c.561G>A	ENSP00000328531.4:p.Ala187=
ENST00000430723.4:c.1233G>A	ENSP00000387657.4:p.Ala411=
ENST00000461280.1:n.868G>A
ENST00000473610.5:n.886G>A
ENST00000532957.5:n.1804G>A
NM_000238.3:c.1581G>A , LRG_288t1:c.1581G>A	NP_000229.1:p.Ala527=
NM_001204798.1:c.561G>A	NP_001191727.1:p.Ala187=
NM_172056.2:c.1581G>A , LRG_288t2:c.1581G>A	NP_742053.1:p.Ala527=
NM_172057.2:c.561G>A , LRG_288t3:c.561G>A	NP_742054.1:p.Ala187=
XM_011516185.1:c.1281G>A	XP_011514487.1:p.Ala427=
XM_011516186.1:c.1581G>A	XP_011514488.1:p.Ala527=
XM_011516185.2:c.1281G>A	XP_011514487.1:p.Ala427=
XM_011516186.3:c.1581G>A	XP_011514488.1:p.Ala527=
XM_017012195.1:c.1431G>A	XP_016867684.1:p.Ala477=
XM_017012196.1:c.1404G>A	XP_016867685.1:p.Ala468=
NM_000238.4:c.1581G>A MANE Select	NP_000229.1:p.Ala527=
NM_001204798.2:c.561G>A	NP_001191727.1:p.Ala187=
NM_172057.3:c.561G>A	NP_742054.1:p.Ala187=