Canonical Allele Identifier: CA458646919

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150656718C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150959630C>A , CM000669.2:g.150959630C>A	GRCh38
NC_000007.13:g.150656718C>A , CM000669.1:g.150656718C>A	GRCh37
NC_000007.12:g.150287651C>A	NCBI36
NG_008916.1:g.23297G>T , LRG_288:g.23297G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1247G>T
ENST00000262186.10:c.414G>T MANE Select	ENSP00000262186.5:p.Val138=
ENST00000262186.9:c.414G>T	ENSP00000262186.5:p.Val138=
ENST00000430723.4:c.234+3G>T	ENSP00000387657.4:n.234+3G>T
ENST00000532957.5:n.637G>T
NM_000238.3:c.414G>T , LRG_288t1:c.414G>T	NP_000229.1:p.Val138=
NM_172056.2:c.414G>T , LRG_288t2:c.414G>T	NP_742053.1:p.Val138=
XM_011516185.1:c.114G>T	XP_011514487.1:p.Val38=
XM_011516186.1:c.414G>T	XP_011514488.1:p.Val138=
XM_011516185.2:c.114G>T	XP_011514487.1:p.Val38=
XM_011516186.3:c.414G>T	XP_011514488.1:p.Val138=
XM_017012195.1:c.264G>T	XP_016867684.1:p.Val88=
XM_017012196.1:c.237G>T	XP_016867685.1:p.Val79=
NM_000238.4:c.414G>T MANE Select	NP_000229.1:p.Val138=