Canonical Allele Identifier: CA369857651

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 3073436
• ClinVar RCV Id: RCV004016442
• MyVariant Identifiers: chr7:g.150648139C>G (hg19) ; chr7:g.150951051C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951051C>G , CM000669.2:g.150951051C>G	GRCh38
NC_000007.13:g.150648139C>G , CM000669.1:g.150648139C>G	GRCh37
NC_000007.12:g.150279072C>G	NCBI36
NG_008916.1:g.31876G>C , LRG_288:g.31876G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1313G>C
ENST00000683359.1:n.139G>C
ENST00000684241.1:n.2848G>C
ENST00000262186.10:c.2015G>C MANE Select	ENSP00000262186.5:p.Arg672Pro
ENST00000330883.9:c.995G>C	ENSP00000328531.4:p.Arg332Pro
ENST00000262186.9:c.2015G>C	ENSP00000262186.5:p.Arg672Pro
ENST00000330883.8:c.995G>C	ENSP00000328531.4:p.Arg332Pro
ENST00000430723.4:c.1667G>C	ENSP00000387657.4:p.Arg556Pro
ENST00000461280.1:n.1302G>C
ENST00000473610.5:n.1647G>C
ENST00000532957.5:n.2238G>C
NM_000238.3:c.2015G>C , LRG_288t1:c.2015G>C	NP_000229.1:p.Arg672Pro
NM_001204798.1:c.995G>C	NP_001191727.1:p.Arg332Pro
NM_172056.2:c.2015G>C , LRG_288t2:c.2015G>C	NP_742053.1:p.Arg672Pro
NM_172057.2:c.995G>C , LRG_288t3:c.995G>C	NP_742054.1:p.Arg332Pro
XM_011516185.1:c.1715G>C	XP_011514487.1:p.Arg572Pro
XM_011516186.1:c.2015G>C	XP_011514488.1:p.Arg672Pro
XM_011516185.2:c.1715G>C	XP_011514487.1:p.Arg572Pro
XM_011516186.3:c.2015G>C	XP_011514488.1:p.Arg672Pro
XM_017012195.1:c.1865G>C	XP_016867684.1:p.Arg622Pro
XM_017012196.1:c.1838G>C	XP_016867685.1:p.Arg613Pro
NM_000238.4:c.2015G>C MANE Select	NP_000229.1:p.Arg672Pro
NM_001204798.2:c.995G>C	NP_001191727.1:p.Arg332Pro
NM_172057.3:c.995G>C	NP_742054.1:p.Arg332Pro