Canonical Allele Identifier: CA369857899

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150648596T>A (hg19) ; chr7:g.150951508T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951508T>A , CM000669.2:g.150951508T>A	GRCh38
NC_000007.13:g.150648596T>A , CM000669.1:g.150648596T>A	GRCh37
NC_000007.12:g.150279529T>A	NCBI36
NG_008916.1:g.31419A>T , LRG_288:g.31419A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.1183A>T
ENST00000683359.1:n.9A>T
ENST00000684241.1:n.2718A>T
ENST00000262186.10:c.1885A>T MANE Select	ENSP00000262186.5:p.Asn629Tyr
ENST00000330883.9:c.865A>T	ENSP00000328531.4:p.Asn289Tyr
ENST00000262186.9:c.1885A>T	ENSP00000262186.5:p.Asn629Tyr
ENST00000330883.8:c.865A>T	ENSP00000328531.4:p.Asn289Tyr
ENST00000430723.4:c.1537A>T	ENSP00000387657.4:p.Asn513Tyr
ENST00000461280.1:n.1172A>T
ENST00000473610.5:n.1190A>T
ENST00000532957.5:n.2108A>T
NM_000238.3:c.1885A>T , LRG_288t1:c.1885A>T	NP_000229.1:p.Asn629Tyr
NM_001204798.1:c.865A>T	NP_001191727.1:p.Asn289Tyr
NM_172056.2:c.1885A>T , LRG_288t2:c.1885A>T	NP_742053.1:p.Asn629Tyr
NM_172057.2:c.865A>T , LRG_288t3:c.865A>T	NP_742054.1:p.Asn289Tyr
XM_011516185.1:c.1585A>T	XP_011514487.1:p.Asn529Tyr
XM_011516186.1:c.1885A>T	XP_011514488.1:p.Asn629Tyr
XM_011516185.2:c.1585A>T	XP_011514487.1:p.Asn529Tyr
XM_011516186.3:c.1885A>T	XP_011514488.1:p.Asn629Tyr
XM_017012195.1:c.1735A>T	XP_016867684.1:p.Asn579Tyr
XM_017012196.1:c.1708A>T	XP_016867685.1:p.Asn570Tyr
NM_000238.4:c.1885A>T MANE Select	NP_000229.1:p.Asn629Tyr
NM_001204798.2:c.865A>T	NP_001191727.1:p.Asn289Tyr
NM_172057.3:c.865A>T	NP_742054.1:p.Asn289Tyr