Canonical Allele Identifier: CA369859817

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150649664A>C (hg19) ; chr7:g.150952576A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952576A>C , CM000669.2:g.150952576A>C	GRCh38
NC_000007.13:g.150649664A>C , CM000669.1:g.150649664A>C	GRCh37
NC_000007.12:g.150280597A>C	NCBI36
NG_008916.1:g.30351T>G , LRG_288:g.30351T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.704T>G
ENST00000684116.1:n.299T>G
ENST00000684241.1:n.2239T>G
ENST00000262186.10:c.1406T>G MANE Select	ENSP00000262186.5:p.Ile469Ser
ENST00000330883.9:c.386T>G	ENSP00000328531.4:p.Ile129Ser
ENST00000262186.9:c.1406T>G	ENSP00000262186.5:p.Ile469Ser
ENST00000330883.8:c.386T>G	ENSP00000328531.4:p.Ile129Ser
ENST00000430723.4:c.1058T>G	ENSP00000387657.4:p.Ile353Ser
ENST00000461280.1:n.693T>G
ENST00000473610.5:n.711T>G
ENST00000532957.5:n.1629T>G
NM_000238.3:c.1406T>G , LRG_288t1:c.1406T>G	NP_000229.1:p.Ile469Ser
NM_001204798.1:c.386T>G	NP_001191727.1:p.Ile129Ser
NM_172056.2:c.1406T>G , LRG_288t2:c.1406T>G	NP_742053.1:p.Ile469Ser
NM_172057.2:c.386T>G , LRG_288t3:c.386T>G	NP_742054.1:p.Ile129Ser
XM_011516185.1:c.1106T>G	XP_011514487.1:p.Ile369Ser
XM_011516186.1:c.1406T>G	XP_011514488.1:p.Ile469Ser
XM_011516185.2:c.1106T>G	XP_011514487.1:p.Ile369Ser
XM_011516186.3:c.1406T>G	XP_011514488.1:p.Ile469Ser
XM_017012195.1:c.1256T>G	XP_016867684.1:p.Ile419Ser
XM_017012196.1:c.1229T>G	XP_016867685.1:p.Ile410Ser
NM_000238.4:c.1406T>G MANE Select	NP_000229.1:p.Ile469Ser
NM_001204798.2:c.386T>G	NP_001191727.1:p.Ile129Ser
NM_172057.3:c.386T>G	NP_742054.1:p.Ile129Ser