Canonical Allele Identifier: CA369861619

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150654479A>C (hg19) ; chr7:g.150957391A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150957391A>C , CM000669.2:g.150957391A>C	GRCh38
NC_000007.13:g.150654479A>C , CM000669.1:g.150654479A>C	GRCh37
NC_000007.12:g.150285412A>C	NCBI36
NG_008916.1:g.25536T>G , LRG_288:g.25536T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.1861T>G
ENST00000262186.10:c.1028T>G MANE Select	ENSP00000262186.5:p.Leu343Arg
ENST00000262186.9:c.1028T>G	ENSP00000262186.5:p.Leu343Arg
ENST00000430723.4:c.680T>G	ENSP00000387657.4:p.Leu227Arg
ENST00000532957.5:n.1251T>G
NM_000238.3:c.1028T>G , LRG_288t1:c.1028T>G	NP_000229.1:p.Leu343Arg
NM_172056.2:c.1028T>G , LRG_288t2:c.1028T>G	NP_742053.1:p.Leu343Arg
XM_011516185.1:c.728T>G	XP_011514487.1:p.Leu243Arg
XM_011516186.1:c.1028T>G	XP_011514488.1:p.Leu343Arg
XM_011516185.2:c.728T>G	XP_011514487.1:p.Leu243Arg
XM_011516186.3:c.1028T>G	XP_011514488.1:p.Leu343Arg
XM_017012195.1:c.878T>G	XP_016867684.1:p.Leu293Arg
XM_017012196.1:c.851T>G	XP_016867685.1:p.Leu284Arg
NM_000238.4:c.1028T>G MANE Select	NP_000229.1:p.Leu343Arg