Canonical Allele Identifier: CA169077527

Gene: KCNH2

Linked Data

• dbSNP Id: rs267601415
• MyVariant Identifiers: chr7:g.150649719G>A (hg19) ; chr7:g.150952631G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952631G>A , CM000669.2:g.150952631G>A	GRCh38
NC_000007.13:g.150649719G>A , CM000669.1:g.150649719G>A	GRCh37
NC_000007.12:g.150280652G>A	NCBI36
NG_008916.1:g.30296C>T , LRG_288:g.30296C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.649C>T
ENST00000684116.1:n.244C>T
ENST00000684241.1:n.2184C>T
ENST00000262186.10:c.1351C>T MANE Select	ENSP00000262186.5:p.Pro451Ser
ENST00000330883.9:c.331C>T	ENSP00000328531.4:p.Pro111Ser
ENST00000262186.9:c.1351C>T	ENSP00000262186.5:p.Pro451Ser
ENST00000330883.8:c.331C>T	ENSP00000328531.4:p.Pro111Ser
ENST00000430723.4:c.1003C>T	ENSP00000387657.4:p.Pro335Ser
ENST00000461280.1:n.638C>T
ENST00000473610.5:n.656C>T
ENST00000532957.5:n.1574C>T
NM_000238.3:c.1351C>T , LRG_288t1:c.1351C>T	NP_000229.1:p.Pro451Ser
NM_001204798.1:c.331C>T	NP_001191727.1:p.Pro111Ser
NM_172056.2:c.1351C>T , LRG_288t2:c.1351C>T	NP_742053.1:p.Pro451Ser
NM_172057.2:c.331C>T , LRG_288t3:c.331C>T	NP_742054.1:p.Pro111Ser
XM_011516185.1:c.1051C>T	XP_011514487.1:p.Pro351Ser
XM_011516186.1:c.1351C>T	XP_011514488.1:p.Pro451Ser
XM_011516185.2:c.1051C>T	XP_011514487.1:p.Pro351Ser
XM_011516186.3:c.1351C>T	XP_011514488.1:p.Pro451Ser
XM_017012195.1:c.1201C>T	XP_016867684.1:p.Pro401Ser
XM_017012196.1:c.1174C>T	XP_016867685.1:p.Pro392Ser
NM_000238.4:c.1351C>T MANE Select	NP_000229.1:p.Pro451Ser
NM_001204798.2:c.331C>T	NP_001191727.1:p.Pro111Ser
NM_172057.3:c.331C>T	NP_742054.1:p.Pro111Ser