Canonical Allele Identifier: CA458871467

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 2716190
• ClinVar RCV Id: RCV003534149
• MyVariant Identifiers: chr7:g.150648579G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951491G>T , CM000669.2:g.150951491G>T	GRCh38
NC_000007.13:g.150648579G>T , CM000669.1:g.150648579G>T	GRCh37
NC_000007.12:g.150279512G>T	NCBI36
NG_008916.1:g.31436C>A , LRG_288:g.31436C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1200C>A
ENST00000683359.1:n.26C>A
ENST00000684241.1:n.2735C>A
ENST00000262186.10:c.1902C>A MANE Select	ENSP00000262186.5:p.Thr634=
ENST00000330883.9:c.882C>A	ENSP00000328531.4:p.Thr294=
ENST00000262186.9:c.1902C>A	ENSP00000262186.5:p.Thr634=
ENST00000330883.8:c.882C>A	ENSP00000328531.4:p.Thr294=
ENST00000430723.4:c.1554C>A	ENSP00000387657.4:p.Thr518=
ENST00000461280.1:n.1189C>A
ENST00000473610.5:n.1207C>A
ENST00000532957.5:n.2125C>A
NM_000238.3:c.1902C>A , LRG_288t1:c.1902C>A	NP_000229.1:p.Thr634=
NM_001204798.1:c.882C>A	NP_001191727.1:p.Thr294=
NM_172056.2:c.1902C>A , LRG_288t2:c.1902C>A	NP_742053.1:p.Thr634=
NM_172057.2:c.882C>A , LRG_288t3:c.882C>A	NP_742054.1:p.Thr294=
XM_011516185.1:c.1602C>A	XP_011514487.1:p.Thr534=
XM_011516186.1:c.1902C>A	XP_011514488.1:p.Thr634=
XM_011516185.2:c.1602C>A	XP_011514487.1:p.Thr534=
XM_011516186.3:c.1902C>A	XP_011514488.1:p.Thr634=
XM_017012195.1:c.1752C>A	XP_016867684.1:p.Thr584=
XM_017012196.1:c.1725C>A	XP_016867685.1:p.Thr575=
NM_000238.4:c.1902C>A MANE Select	NP_000229.1:p.Thr634=
NM_001204798.2:c.882C>A	NP_001191727.1:p.Thr294=
NM_172057.3:c.882C>A	NP_742054.1:p.Thr294=