Canonical Allele Identifier: CA369861598

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150654468G>T (hg19) ; chr7:g.150957380G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150957380G>T , CM000669.2:g.150957380G>T	GRCh38
NC_000007.13:g.150654468G>T , CM000669.1:g.150654468G>T	GRCh37
NC_000007.12:g.150285401G>T	NCBI36
NG_008916.1:g.25547C>A , LRG_288:g.25547C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.1872C>A
ENST00000262186.10:c.1039C>A MANE Select	ENSP00000262186.5:p.Pro347Thr
ENST00000262186.9:c.1039C>A	ENSP00000262186.5:p.Pro347Thr
ENST00000430723.4:c.691C>A	ENSP00000387657.4:p.Pro231Thr
ENST00000532957.5:n.1262C>A
NM_000238.3:c.1039C>A , LRG_288t1:c.1039C>A	NP_000229.1:p.Pro347Thr
NM_172056.2:c.1039C>A , LRG_288t2:c.1039C>A	NP_742053.1:p.Pro347Thr
XM_011516185.1:c.739C>A	XP_011514487.1:p.Pro247Thr
XM_011516186.1:c.1039C>A	XP_011514488.1:p.Pro347Thr
XM_011516185.2:c.739C>A	XP_011514487.1:p.Pro247Thr
XM_011516186.3:c.1039C>A	XP_011514488.1:p.Pro347Thr
XM_017012195.1:c.889C>A	XP_016867684.1:p.Pro297Thr
XM_017012196.1:c.862C>A	XP_016867685.1:p.Pro288Thr
NM_000238.4:c.1039C>A MANE Select	NP_000229.1:p.Pro347Thr