Canonical Allele Identifier: CA458645455

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150648156C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951068C>G , CM000669.2:g.150951068C>G	GRCh38
NC_000007.13:g.150648156C>G , CM000669.1:g.150648156C>G	GRCh37
NC_000007.12:g.150279089C>G	NCBI36
NG_008916.1:g.31859G>C , LRG_288:g.31859G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1296G>C
ENST00000683359.1:n.122G>C
ENST00000684241.1:n.2831G>C
ENST00000262186.10:c.1998G>C MANE Select	ENSP00000262186.5:p.Leu666=
ENST00000330883.9:c.978G>C	ENSP00000328531.4:p.Leu326=
ENST00000262186.9:c.1998G>C	ENSP00000262186.5:p.Leu666=
ENST00000330883.8:c.978G>C	ENSP00000328531.4:p.Leu326=
ENST00000430723.4:c.1650G>C	ENSP00000387657.4:p.Leu550=
ENST00000461280.1:n.1285G>C
ENST00000473610.5:n.1630G>C
ENST00000532957.5:n.2221G>C
NM_000238.3:c.1998G>C , LRG_288t1:c.1998G>C	NP_000229.1:p.Leu666=
NM_001204798.1:c.978G>C	NP_001191727.1:p.Leu326=
NM_172056.2:c.1998G>C , LRG_288t2:c.1998G>C	NP_742053.1:p.Leu666=
NM_172057.2:c.978G>C , LRG_288t3:c.978G>C	NP_742054.1:p.Leu326=
XM_011516185.1:c.1698G>C	XP_011514487.1:p.Leu566=
XM_011516186.1:c.1998G>C	XP_011514488.1:p.Leu666=
XM_011516185.2:c.1698G>C	XP_011514487.1:p.Leu566=
XM_011516186.3:c.1998G>C	XP_011514488.1:p.Leu666=
XM_017012195.1:c.1848G>C	XP_016867684.1:p.Leu616=
XM_017012196.1:c.1821G>C	XP_016867685.1:p.Leu607=
NM_000238.4:c.1998G>C MANE Select	NP_000229.1:p.Leu666=
NM_001204798.2:c.978G>C	NP_001191727.1:p.Leu326=
NM_172057.3:c.978G>C	NP_742054.1:p.Leu326=