Canonical Allele Identifier: CA369860094

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150952715-C-T
• MyVariant Identifiers: chr7:g.150649803C>T (hg19) ; chr7:g.150952715C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952715C>T , CM000669.2:g.150952715C>T	GRCh38
NC_000007.13:g.150649803C>T , CM000669.1:g.150649803C>T	GRCh37
NC_000007.12:g.150280736C>T	NCBI36
NG_008916.1:g.30212G>A , LRG_288:g.30212G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.565G>A
ENST00000684116.1:n.160G>A
ENST00000684241.1:n.2100G>A
ENST00000262186.10:c.1267G>A MANE Select	ENSP00000262186.5:p.Val423Ile
ENST00000330883.9:c.247G>A	ENSP00000328531.4:p.Val83Ile
ENST00000262186.9:c.1267G>A	ENSP00000262186.5:p.Val423Ile
ENST00000330883.8:c.247G>A	ENSP00000328531.4:p.Val83Ile
ENST00000430723.4:c.919G>A	ENSP00000387657.4:p.Val307Ile
ENST00000461280.1:n.554G>A
ENST00000473610.5:n.572G>A
ENST00000532957.5:n.1490G>A
NM_000238.3:c.1267G>A , LRG_288t1:c.1267G>A	NP_000229.1:p.Val423Ile
NM_001204798.1:c.247G>A	NP_001191727.1:p.Val83Ile
NM_172056.2:c.1267G>A , LRG_288t2:c.1267G>A	NP_742053.1:p.Val423Ile
NM_172057.2:c.247G>A , LRG_288t3:c.247G>A	NP_742054.1:p.Val83Ile
XM_011516185.1:c.967G>A	XP_011514487.1:p.Val323Ile
XM_011516186.1:c.1267G>A	XP_011514488.1:p.Val423Ile
XM_011516185.2:c.967G>A	XP_011514487.1:p.Val323Ile
XM_011516186.3:c.1267G>A	XP_011514488.1:p.Val423Ile
XM_017012195.1:c.1117G>A	XP_016867684.1:p.Val373Ile
XM_017012196.1:c.1090G>A	XP_016867685.1:p.Val364Ile
NM_000238.4:c.1267G>A MANE Select	NP_000229.1:p.Val423Ile
NM_001204798.2:c.247G>A	NP_001191727.1:p.Val83Ile
NM_172057.3:c.247G>A	NP_742054.1:p.Val83Ile