Canonical Allele Identifier: CA369856042

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150647291T>G (hg19) ; chr7:g.150950203T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150950203T>G , CM000669.2:g.150950203T>G	GRCh38
NC_000007.13:g.150647291T>G , CM000669.1:g.150647291T>G	GRCh37
NC_000007.12:g.150278224T>G	NCBI36
NG_008916.1:g.32724A>C , LRG_288:g.32724A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1661A>C
ENST00000684241.1:n.3196A>C
ENST00000262186.10:c.2363A>C MANE Select	ENSP00000262186.5:p.Glu788Ala
ENST00000330883.9:c.1343A>C	ENSP00000328531.4:p.Glu448Ala
ENST00000262186.9:c.2363A>C	ENSP00000262186.5:p.Glu788Ala
ENST00000330883.8:c.1343A>C	ENSP00000328531.4:p.Glu448Ala
ENST00000430723.4:c.2015A>C	ENSP00000387657.4:p.Glu672Ala
ENST00000461280.1:n.1650A>C
ENST00000473610.5:n.1995A>C
ENST00000532957.5:n.2586A>C
NM_000238.3:c.2363A>C , LRG_288t1:c.2363A>C	NP_000229.1:p.Glu788Ala
NM_001204798.1:c.1343A>C	NP_001191727.1:p.Glu448Ala
NM_172056.2:c.2363A>C , LRG_288t2:c.2363A>C	NP_742053.1:p.Glu788Ala
NM_172057.2:c.1343A>C , LRG_288t3:c.1343A>C	NP_742054.1:p.Glu448Ala
XM_011516185.1:c.2063A>C	XP_011514487.1:p.Glu688Ala
XM_011516186.1:c.2363A>C	XP_011514488.1:p.Glu788Ala
XM_011516185.2:c.2063A>C	XP_011514487.1:p.Glu688Ala
XM_011516186.3:c.2363A>C	XP_011514488.1:p.Glu788Ala
XM_017012195.1:c.2213A>C	XP_016867684.1:p.Glu738Ala
XM_017012196.1:c.2186A>C	XP_016867685.1:p.Glu729Ala
NM_000238.4:c.2363A>C MANE Select	NP_000229.1:p.Glu788Ala
NM_001204798.2:c.1343A>C	NP_001191727.1:p.Glu448Ala
NM_172057.3:c.1343A>C	NP_742054.1:p.Glu448Ala