Canonical Allele Identifier: CA369863313

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150655504C>G (hg19) ; chr7:g.150958416C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958416C>G , CM000669.2:g.150958416C>G	GRCh38
NC_000007.13:g.150655504C>G , CM000669.1:g.150655504C>G	GRCh37
NC_000007.12:g.150286437C>G	NCBI36
NG_008916.1:g.24511G>C , LRG_288:g.24511G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.1392G>C
ENST00000262186.10:c.559G>C MANE Select	ENSP00000262186.5:p.Gly187Arg
ENST00000262186.9:c.559G>C	ENSP00000262186.5:p.Gly187Arg
ENST00000430723.4:c.235-24G>C	ENSP00000387657.4:n.235-24G>C
ENST00000532957.5:n.782G>C
NM_000238.3:c.559G>C , LRG_288t1:c.559G>C	NP_000229.1:p.Gly187Arg
NM_172056.2:c.559G>C , LRG_288t2:c.559G>C	NP_742053.1:p.Gly187Arg
XM_011516185.1:c.259G>C	XP_011514487.1:p.Gly87Arg
XM_011516186.1:c.559G>C	XP_011514488.1:p.Gly187Arg
XM_011516185.2:c.259G>C	XP_011514487.1:p.Gly87Arg
XM_011516186.3:c.559G>C	XP_011514488.1:p.Gly187Arg
XM_017012195.1:c.409G>C	XP_016867684.1:p.Gly137Arg
XM_017012196.1:c.382G>C	XP_016867685.1:p.Gly128Arg
NM_000238.4:c.559G>C MANE Select	NP_000229.1:p.Gly187Arg