Canonical Allele Identifier: CA458646847

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150655553C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958465C>G , CM000669.2:g.150958465C>G	GRCh38
NC_000007.13:g.150655553C>G , CM000669.1:g.150655553C>G	GRCh37
NC_000007.12:g.150286486C>G	NCBI36
NG_008916.1:g.24462G>C , LRG_288:g.24462G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1343G>C
ENST00000262186.10:c.510G>C MANE Select	ENSP00000262186.5:p.Leu170=
ENST00000262186.9:c.510G>C	ENSP00000262186.5:p.Leu170=
ENST00000430723.4:c.235-73G>C	ENSP00000387657.4:n.235-73G>C
ENST00000532957.5:n.733G>C
NM_000238.3:c.510G>C , LRG_288t1:c.510G>C	NP_000229.1:p.Leu170=
NM_172056.2:c.510G>C , LRG_288t2:c.510G>C	NP_742053.1:p.Leu170=
XM_011516185.1:c.210G>C	XP_011514487.1:p.Leu70=
XM_011516186.1:c.510G>C	XP_011514488.1:p.Leu170=
XM_011516185.2:c.210G>C	XP_011514487.1:p.Leu70=
XM_011516186.3:c.510G>C	XP_011514488.1:p.Leu170=
XM_017012195.1:c.360G>C	XP_016867684.1:p.Leu120=
XM_017012196.1:c.333G>C	XP_016867685.1:p.Leu111=
NM_000238.4:c.510G>C MANE Select	NP_000229.1:p.Leu170=