Canonical Allele Identifier: CA369859892

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150649697A>G (hg19) ; chr7:g.150952609A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952609A>G , CM000669.2:g.150952609A>G	GRCh38
NC_000007.13:g.150649697A>G , CM000669.1:g.150649697A>G	GRCh37
NC_000007.12:g.150280630A>G	NCBI36
NG_008916.1:g.30318T>C , LRG_288:g.30318T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.671T>C
ENST00000684116.1:n.266T>C
ENST00000684241.1:n.2206T>C
ENST00000262186.10:c.1373T>C MANE Select	ENSP00000262186.5:p.Ile458Thr
ENST00000330883.9:c.353T>C	ENSP00000328531.4:p.Ile118Thr
ENST00000262186.9:c.1373T>C	ENSP00000262186.5:p.Ile458Thr
ENST00000330883.8:c.353T>C	ENSP00000328531.4:p.Ile118Thr
ENST00000430723.4:c.1025T>C	ENSP00000387657.4:p.Ile342Thr
ENST00000461280.1:n.660T>C
ENST00000473610.5:n.678T>C
ENST00000532957.5:n.1596T>C
NM_000238.3:c.1373T>C , LRG_288t1:c.1373T>C	NP_000229.1:p.Ile458Thr
NM_001204798.1:c.353T>C	NP_001191727.1:p.Ile118Thr
NM_172056.2:c.1373T>C , LRG_288t2:c.1373T>C	NP_742053.1:p.Ile458Thr
NM_172057.2:c.353T>C , LRG_288t3:c.353T>C	NP_742054.1:p.Ile118Thr
XM_011516185.1:c.1073T>C	XP_011514487.1:p.Ile358Thr
XM_011516186.1:c.1373T>C	XP_011514488.1:p.Ile458Thr
XM_011516185.2:c.1073T>C	XP_011514487.1:p.Ile358Thr
XM_011516186.3:c.1373T>C	XP_011514488.1:p.Ile458Thr
XM_017012195.1:c.1223T>C	XP_016867684.1:p.Ile408Thr
XM_017012196.1:c.1196T>C	XP_016867685.1:p.Ile399Thr
NM_000238.4:c.1373T>C MANE Select	NP_000229.1:p.Ile458Thr
NM_001204798.2:c.353T>C	NP_001191727.1:p.Ile118Thr
NM_172057.3:c.353T>C	NP_742054.1:p.Ile118Thr