Canonical Allele Identifier: CA369856660

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150647478C>T (hg19) ; chr7:g.150950390C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150950390C>T , CM000669.2:g.150950390C>T	GRCh38
NC_000007.13:g.150647478C>T , CM000669.1:g.150647478C>T	GRCh37
NC_000007.12:g.150278411C>T	NCBI36
NG_008916.1:g.32537G>A , LRG_288:g.32537G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1474G>A
ENST00000684241.1:n.3009G>A
ENST00000262186.10:c.2176G>A MANE Select	ENSP00000262186.5:p.Ala726Thr
ENST00000330883.9:c.1156G>A	ENSP00000328531.4:p.Ala386Thr
ENST00000262186.9:c.2176G>A	ENSP00000262186.5:p.Ala726Thr
ENST00000330883.8:c.1156G>A	ENSP00000328531.4:p.Ala386Thr
ENST00000430723.4:c.1828G>A	ENSP00000387657.4:p.Ala610Thr
ENST00000461280.1:n.1463G>A
ENST00000473610.5:n.1808G>A
ENST00000532957.5:n.2399G>A
NM_000238.3:c.2176G>A , LRG_288t1:c.2176G>A	NP_000229.1:p.Ala726Thr
NM_001204798.1:c.1156G>A	NP_001191727.1:p.Ala386Thr
NM_172056.2:c.2176G>A , LRG_288t2:c.2176G>A	NP_742053.1:p.Ala726Thr
NM_172057.2:c.1156G>A , LRG_288t3:c.1156G>A	NP_742054.1:p.Ala386Thr
XM_011516185.1:c.1876G>A	XP_011514487.1:p.Ala626Thr
XM_011516186.1:c.2176G>A	XP_011514488.1:p.Ala726Thr
XM_011516185.2:c.1876G>A	XP_011514487.1:p.Ala626Thr
XM_011516186.3:c.2176G>A	XP_011514488.1:p.Ala726Thr
XM_017012195.1:c.2026G>A	XP_016867684.1:p.Ala676Thr
XM_017012196.1:c.1999G>A	XP_016867685.1:p.Ala667Thr
NM_000238.4:c.2176G>A MANE Select	NP_000229.1:p.Ala726Thr
NM_001204798.2:c.1156G>A	NP_001191727.1:p.Ala386Thr
NM_172057.3:c.1156G>A	NP_742054.1:p.Ala386Thr