Canonical Allele Identifier: CA369860172

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150649842A>C (hg19) ; chr7:g.150952754A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952754A>C , CM000669.2:g.150952754A>C	GRCh38
NC_000007.13:g.150649842A>C , CM000669.1:g.150649842A>C	GRCh37
NC_000007.12:g.150280775A>C	NCBI36
NG_008916.1:g.30173T>G , LRG_288:g.30173T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.526T>G
ENST00000684116.1:n.121T>G
ENST00000684241.1:n.2061T>G
ENST00000262186.10:c.1228T>G MANE Select	ENSP00000262186.5:p.Trp410Gly
ENST00000330883.9:c.208T>G	ENSP00000328531.4:p.Trp70Gly
ENST00000262186.9:c.1228T>G	ENSP00000262186.5:p.Trp410Gly
ENST00000330883.8:c.208T>G	ENSP00000328531.4:p.Trp70Gly
ENST00000430723.4:c.880T>G	ENSP00000387657.4:p.Trp294Gly
ENST00000461280.1:n.515T>G
ENST00000473610.5:n.533T>G
ENST00000532957.5:n.1451T>G
NM_000238.3:c.1228T>G , LRG_288t1:c.1228T>G	NP_000229.1:p.Trp410Gly
NM_001204798.1:c.208T>G	NP_001191727.1:p.Trp70Gly
NM_172056.2:c.1228T>G , LRG_288t2:c.1228T>G	NP_742053.1:p.Trp410Gly
NM_172057.2:c.208T>G , LRG_288t3:c.208T>G	NP_742054.1:p.Trp70Gly
XM_011516185.1:c.928T>G	XP_011514487.1:p.Trp310Gly
XM_011516186.1:c.1228T>G	XP_011514488.1:p.Trp410Gly
XM_011516185.2:c.928T>G	XP_011514487.1:p.Trp310Gly
XM_011516186.3:c.1228T>G	XP_011514488.1:p.Trp410Gly
XM_017012195.1:c.1078T>G	XP_016867684.1:p.Trp360Gly
XM_017012196.1:c.1051T>G	XP_016867685.1:p.Trp351Gly
NM_000238.4:c.1228T>G MANE Select	NP_000229.1:p.Trp410Gly
NM_001204798.2:c.208T>G	NP_001191727.1:p.Trp70Gly
NM_172057.3:c.208T>G	NP_742054.1:p.Trp70Gly