Canonical Allele Identifier: CA369857951

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150648629T>A (hg19) ; chr7:g.150951541T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951541T>A , CM000669.2:g.150951541T>A	GRCh38
NC_000007.13:g.150648629T>A , CM000669.1:g.150648629T>A	GRCh37
NC_000007.12:g.150279562T>A	NCBI36
NG_008916.1:g.31386A>T , LRG_288:g.31386A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1150A>T
ENST00000684241.1:n.2685A>T
ENST00000262186.10:c.1852A>T MANE Select	ENSP00000262186.5:p.Thr618Ser
ENST00000330883.9:c.832A>T	ENSP00000328531.4:p.Thr278Ser
ENST00000262186.9:c.1852A>T	ENSP00000262186.5:p.Thr618Ser
ENST00000330883.8:c.832A>T	ENSP00000328531.4:p.Thr278Ser
ENST00000430723.4:c.1504A>T	ENSP00000387657.4:p.Thr502Ser
ENST00000461280.1:n.1139A>T
ENST00000473610.5:n.1157A>T
ENST00000532957.5:n.2075A>T
NM_000238.3:c.1852A>T , LRG_288t1:c.1852A>T	NP_000229.1:p.Thr618Ser
NM_001204798.1:c.832A>T	NP_001191727.1:p.Thr278Ser
NM_172056.2:c.1852A>T , LRG_288t2:c.1852A>T	NP_742053.1:p.Thr618Ser
NM_172057.2:c.832A>T , LRG_288t3:c.832A>T	NP_742054.1:p.Thr278Ser
XM_011516185.1:c.1552A>T	XP_011514487.1:p.Thr518Ser
XM_011516186.1:c.1852A>T	XP_011514488.1:p.Thr618Ser
XM_011516185.2:c.1552A>T	XP_011514487.1:p.Thr518Ser
XM_011516186.3:c.1852A>T	XP_011514488.1:p.Thr618Ser
XM_017012195.1:c.1702A>T	XP_016867684.1:p.Thr568Ser
XM_017012196.1:c.1675A>T	XP_016867685.1:p.Thr559Ser
NM_000238.4:c.1852A>T MANE Select	NP_000229.1:p.Thr618Ser
NM_001204798.2:c.832A>T	NP_001191727.1:p.Thr278Ser
NM_172057.3:c.832A>T	NP_742054.1:p.Thr278Ser