Canonical Allele Identifier: CA369858060

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150648689T>A (hg19) ; chr7:g.150951601T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951601T>A , CM000669.2:g.150951601T>A	GRCh38
NC_000007.13:g.150648689T>A , CM000669.1:g.150648689T>A	GRCh37
NC_000007.12:g.150279622T>A	NCBI36
NG_008916.1:g.31326A>T , LRG_288:g.31326A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1090A>T
ENST00000684241.1:n.2625A>T
ENST00000262186.10:c.1792A>T MANE Select	ENSP00000262186.5:p.Asn598Tyr
ENST00000330883.9:c.772A>T	ENSP00000328531.4:p.Asn258Tyr
ENST00000262186.9:c.1792A>T	ENSP00000262186.5:p.Asn598Tyr
ENST00000330883.8:c.772A>T	ENSP00000328531.4:p.Asn258Tyr
ENST00000430723.4:c.1444A>T	ENSP00000387657.4:p.Asn482Tyr
ENST00000461280.1:n.1079A>T
ENST00000473610.5:n.1097A>T
ENST00000532957.5:n.2015A>T
NM_000238.3:c.1792A>T , LRG_288t1:c.1792A>T	NP_000229.1:p.Asn598Tyr
NM_001204798.1:c.772A>T	NP_001191727.1:p.Asn258Tyr
NM_172056.2:c.1792A>T , LRG_288t2:c.1792A>T	NP_742053.1:p.Asn598Tyr
NM_172057.2:c.772A>T , LRG_288t3:c.772A>T	NP_742054.1:p.Asn258Tyr
XM_011516185.1:c.1492A>T	XP_011514487.1:p.Asn498Tyr
XM_011516186.1:c.1792A>T	XP_011514488.1:p.Asn598Tyr
XM_011516185.2:c.1492A>T	XP_011514487.1:p.Asn498Tyr
XM_011516186.3:c.1792A>T	XP_011514488.1:p.Asn598Tyr
XM_017012195.1:c.1642A>T	XP_016867684.1:p.Asn548Tyr
XM_017012196.1:c.1615A>T	XP_016867685.1:p.Asn539Tyr
NM_000238.4:c.1792A>T MANE Select	NP_000229.1:p.Asn598Tyr
NM_001204798.2:c.772A>T	NP_001191727.1:p.Asn258Tyr
NM_172057.3:c.772A>T	NP_742054.1:p.Asn258Tyr