Canonical Allele Identifier: CA369855794

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150647163T>G (hg19) ; chr7:g.150950075T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150950075T>G , CM000669.2:g.150950075T>G	GRCh38
NC_000007.13:g.150647163T>G , CM000669.1:g.150647163T>G	GRCh37
NC_000007.12:g.150278096T>G	NCBI36
NG_008916.1:g.32852A>C , LRG_288:g.32852A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1789A>C
ENST00000684241.1:n.3231+93A>C
ENST00000262186.10:c.2398+93A>C MANE Select	ENSP00000262186.5:n.2398+93A>C
ENST00000330883.9:c.1378+93A>C	ENSP00000328531.4:n.1378+93A>C
ENST00000262186.9:c.2398+93A>C	ENSP00000262186.5:n.2398+93A>C
ENST00000330883.8:c.1378+93A>C	ENSP00000328531.4:n.1378+93A>C
ENST00000430723.4:c.2143A>C	ENSP00000387657.4:p.Thr715Pro
ENST00000461280.1:n.1778A>C
ENST00000473610.5:n.2123A>C
ENST00000532957.5:n.2714A>C
NM_000238.3:c.2398+93A>C , LRG_288t1:c.2398+93A>C	NP_000229.1:n.2398+93A>C
NM_001204798.1:c.1471A>C	NP_001191727.1:p.Thr491Pro
NM_172056.2:c.2491A>C , LRG_288t2:c.2491A>C	NP_742053.1:p.Thr831Pro
NM_172057.2:c.1378+93A>C , LRG_288t3:c.1378+93A>C	NP_742054.1:n.1378+93A>C
XM_011516185.1:c.2098+93A>C	XP_011514487.1:n.2098+93A>C
XM_011516186.1:c.2398+93A>C	XP_011514488.1:n.2398+93A>C
XM_011516185.2:c.2098+93A>C	XP_011514487.1:n.2098+93A>C
XM_011516186.3:c.2398+93A>C	XP_011514488.1:n.2398+93A>C
XM_017012195.1:c.2248+93A>C	XP_016867684.1:n.2248+93A>C
XM_017012196.1:c.2221+93A>C	XP_016867685.1:n.2221+93A>C
NM_000238.4:c.2398+93A>C MANE Select	NP_000229.1:n.2398+93A>C
NM_001204798.2:c.1471A>C	NP_001191727.1:p.Thr491Pro
NM_172057.3:c.1378+93A>C	NP_742054.1:n.1378+93A>C