Canonical Allele Identifier: CA458871421

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150647464C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150950376C>G , CM000669.2:g.150950376C>G	GRCh38
NC_000007.13:g.150647464C>G , CM000669.1:g.150647464C>G	GRCh37
NC_000007.12:g.150278397C>G	NCBI36
NG_008916.1:g.32551G>C , LRG_288:g.32551G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1488G>C
ENST00000684241.1:n.3023G>C
ENST00000262186.10:c.2190G>C MANE Select	ENSP00000262186.5:p.Leu730=
ENST00000330883.9:c.1170G>C	ENSP00000328531.4:p.Leu390=
ENST00000262186.9:c.2190G>C	ENSP00000262186.5:p.Leu730=
ENST00000330883.8:c.1170G>C	ENSP00000328531.4:p.Leu390=
ENST00000430723.4:c.1842G>C	ENSP00000387657.4:p.Leu614=
ENST00000461280.1:n.1477G>C
ENST00000473610.5:n.1822G>C
ENST00000532957.5:n.2413G>C
NM_000238.3:c.2190G>C , LRG_288t1:c.2190G>C	NP_000229.1:p.Leu730=
NM_001204798.1:c.1170G>C	NP_001191727.1:p.Leu390=
NM_172056.2:c.2190G>C , LRG_288t2:c.2190G>C	NP_742053.1:p.Leu730=
NM_172057.2:c.1170G>C , LRG_288t3:c.1170G>C	NP_742054.1:p.Leu390=
XM_011516185.1:c.1890G>C	XP_011514487.1:p.Leu630=
XM_011516186.1:c.2190G>C	XP_011514488.1:p.Leu730=
XM_011516185.2:c.1890G>C	XP_011514487.1:p.Leu630=
XM_011516186.3:c.2190G>C	XP_011514488.1:p.Leu730=
XM_017012195.1:c.2040G>C	XP_016867684.1:p.Leu680=
XM_017012196.1:c.2013G>C	XP_016867685.1:p.Leu671=
NM_000238.4:c.2190G>C MANE Select	NP_000229.1:p.Leu730=
NM_001204798.2:c.1170G>C	NP_001191727.1:p.Leu390=
NM_172057.3:c.1170G>C	NP_742054.1:p.Leu390=