Canonical Allele Identifier: CA369860221

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150649865T>G (hg19) ; chr7:g.150952777T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952777T>G , CM000669.2:g.150952777T>G	GRCh38
NC_000007.13:g.150649865T>G , CM000669.1:g.150649865T>G	GRCh37
NC_000007.12:g.150280798T>G	NCBI36
NG_008916.1:g.30150A>C , LRG_288:g.30150A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.503A>C
ENST00000684116.1:n.98A>C
ENST00000684241.1:n.2038A>C
ENST00000262186.10:c.1205A>C MANE Select	ENSP00000262186.5:p.His402Pro
ENST00000330883.9:c.185A>C	ENSP00000328531.4:p.His62Pro
ENST00000262186.9:c.1205A>C	ENSP00000262186.5:p.His402Pro
ENST00000330883.8:c.185A>C	ENSP00000328531.4:p.His62Pro
ENST00000430723.4:c.857A>C	ENSP00000387657.4:p.His286Pro
ENST00000461280.1:n.492A>C
ENST00000473610.5:n.510A>C
ENST00000532957.5:n.1428A>C
NM_000238.3:c.1205A>C , LRG_288t1:c.1205A>C	NP_000229.1:p.His402Pro
NM_001204798.1:c.185A>C	NP_001191727.1:p.His62Pro
NM_172056.2:c.1205A>C , LRG_288t2:c.1205A>C	NP_742053.1:p.His402Pro
NM_172057.2:c.185A>C , LRG_288t3:c.185A>C	NP_742054.1:p.His62Pro
XM_011516185.1:c.905A>C	XP_011514487.1:p.His302Pro
XM_011516186.1:c.1205A>C	XP_011514488.1:p.His402Pro
XM_011516185.2:c.905A>C	XP_011514487.1:p.His302Pro
XM_011516186.3:c.1205A>C	XP_011514488.1:p.His402Pro
XM_017012195.1:c.1055A>C	XP_016867684.1:p.His352Pro
XM_017012196.1:c.1028A>C	XP_016867685.1:p.His343Pro
NM_000238.4:c.1205A>C MANE Select	NP_000229.1:p.His402Pro
NM_001204798.2:c.185A>C	NP_001191727.1:p.His62Pro
NM_172057.3:c.185A>C	NP_742054.1:p.His62Pro