Canonical Allele Identifier: CA369862739

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150958262-C-A
• MyVariant Identifiers: chr7:g.150655350C>A (hg19) ; chr7:g.150958262C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958262C>A , CM000669.2:g.150958262C>A	GRCh38
NC_000007.13:g.150655350C>A , CM000669.1:g.150655350C>A	GRCh37
NC_000007.12:g.150286283C>A	NCBI36
NG_008916.1:g.24665G>T , LRG_288:g.24665G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1546G>T
ENST00000262186.10:c.713G>T MANE Select	ENSP00000262186.5:p.Gly238Val
ENST00000262186.9:c.713G>T	ENSP00000262186.5:p.Gly238Val
ENST00000430723.4:c.365G>T	ENSP00000387657.4:p.Gly122Val
ENST00000532957.5:n.936G>T
NM_000238.3:c.713G>T , LRG_288t1:c.713G>T	NP_000229.1:p.Gly238Val
NM_172056.2:c.713G>T , LRG_288t2:c.713G>T	NP_742053.1:p.Gly238Val
XM_011516185.1:c.413G>T	XP_011514487.1:p.Gly138Val
XM_011516186.1:c.713G>T	XP_011514488.1:p.Gly238Val
XM_011516185.2:c.413G>T	XP_011514487.1:p.Gly138Val
XM_011516186.3:c.713G>T	XP_011514488.1:p.Gly238Val
XM_017012195.1:c.563G>T	XP_016867684.1:p.Gly188Val
XM_017012196.1:c.536G>T	XP_016867685.1:p.Gly179Val
NM_000238.4:c.713G>T MANE Select	NP_000229.1:p.Gly238Val