Canonical Allele Identifier: CA369860242

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150649876C>G (hg19) ; chr7:g.150952788C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952788C>G , CM000669.2:g.150952788C>G	GRCh38
NC_000007.13:g.150649876C>G , CM000669.1:g.150649876C>G	GRCh37
NC_000007.12:g.150280809C>G	NCBI36
NG_008916.1:g.30139G>C , LRG_288:g.30139G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.492G>C
ENST00000684116.1:n.87G>C
ENST00000684241.1:n.2027G>C
ENST00000262186.10:c.1194G>C MANE Select	ENSP00000262186.5:p.Trp398Cys
ENST00000330883.9:c.174G>C	ENSP00000328531.4:p.Trp58Cys
ENST00000262186.9:c.1194G>C	ENSP00000262186.5:p.Trp398Cys
ENST00000330883.8:c.174G>C	ENSP00000328531.4:p.Trp58Cys
ENST00000430723.4:c.846G>C	ENSP00000387657.4:p.Trp282Cys
ENST00000461280.1:n.481G>C
ENST00000473610.5:n.499G>C
ENST00000532957.5:n.1417G>C
NM_000238.3:c.1194G>C , LRG_288t1:c.1194G>C	NP_000229.1:p.Trp398Cys
NM_001204798.1:c.174G>C	NP_001191727.1:p.Trp58Cys
NM_172056.2:c.1194G>C , LRG_288t2:c.1194G>C	NP_742053.1:p.Trp398Cys
NM_172057.2:c.174G>C , LRG_288t3:c.174G>C	NP_742054.1:p.Trp58Cys
XM_011516185.1:c.894G>C	XP_011514487.1:p.Trp298Cys
XM_011516186.1:c.1194G>C	XP_011514488.1:p.Trp398Cys
XM_011516185.2:c.894G>C	XP_011514487.1:p.Trp298Cys
XM_011516186.3:c.1194G>C	XP_011514488.1:p.Trp398Cys
XM_017012195.1:c.1044G>C	XP_016867684.1:p.Trp348Cys
XM_017012196.1:c.1017G>C	XP_016867685.1:p.Trp339Cys
NM_000238.4:c.1194G>C MANE Select	NP_000229.1:p.Trp398Cys
NM_001204798.2:c.174G>C	NP_001191727.1:p.Trp58Cys
NM_172057.3:c.174G>C	NP_742054.1:p.Trp58Cys