Canonical Allele Identifier: CA369857892

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150648590A>T (hg19) ; chr7:g.150951502A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951502A>T , CM000669.2:g.150951502A>T	GRCh38
NC_000007.13:g.150648590A>T , CM000669.1:g.150648590A>T	GRCh37
NC_000007.12:g.150279523A>T	NCBI36
NG_008916.1:g.31425T>A , LRG_288:g.31425T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1189T>A
ENST00000683359.1:n.15T>A
ENST00000684241.1:n.2724T>A
ENST00000262186.10:c.1891T>A MANE Select	ENSP00000262186.5:p.Ser631Thr
ENST00000330883.9:c.871T>A	ENSP00000328531.4:p.Ser291Thr
ENST00000262186.9:c.1891T>A	ENSP00000262186.5:p.Ser631Thr
ENST00000330883.8:c.871T>A	ENSP00000328531.4:p.Ser291Thr
ENST00000430723.4:c.1543T>A	ENSP00000387657.4:p.Ser515Thr
ENST00000461280.1:n.1178T>A
ENST00000473610.5:n.1196T>A
ENST00000532957.5:n.2114T>A
NM_000238.3:c.1891T>A , LRG_288t1:c.1891T>A	NP_000229.1:p.Ser631Thr
NM_001204798.1:c.871T>A	NP_001191727.1:p.Ser291Thr
NM_172056.2:c.1891T>A , LRG_288t2:c.1891T>A	NP_742053.1:p.Ser631Thr
NM_172057.2:c.871T>A , LRG_288t3:c.871T>A	NP_742054.1:p.Ser291Thr
XM_011516185.1:c.1591T>A	XP_011514487.1:p.Ser531Thr
XM_011516186.1:c.1891T>A	XP_011514488.1:p.Ser631Thr
XM_011516185.2:c.1591T>A	XP_011514487.1:p.Ser531Thr
XM_011516186.3:c.1891T>A	XP_011514488.1:p.Ser631Thr
XM_017012195.1:c.1741T>A	XP_016867684.1:p.Ser581Thr
XM_017012196.1:c.1714T>A	XP_016867685.1:p.Ser572Thr
NM_000238.4:c.1891T>A MANE Select	NP_000229.1:p.Ser631Thr
NM_001204798.2:c.871T>A	NP_001191727.1:p.Ser291Thr
NM_172057.3:c.871T>A	NP_742054.1:p.Ser291Thr