Canonical Allele Identifier: CA005538

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 200730
• ClinVar RCV Id: RCV000182024
• dbSNP Id: rs794728480
• MyVariant Identifiers: chr7:g.150648679C>T (hg19) ; chr7:g.150951591C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951591C>T , CM000669.2:g.150951591C>T	GRCh38
NC_000007.13:g.150648679C>T , CM000669.1:g.150648679C>T	GRCh37
NC_000007.12:g.150279612C>T	NCBI36
NG_008916.1:g.31336G>A , LRG_288:g.31336G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1100G>A
ENST00000684241.1:n.2635G>A
ENST00000262186.10:c.1802G>A MANE Select	ENSP00000262186.5:p.Gly601Asp
ENST00000330883.9:c.782G>A	ENSP00000328531.4:p.Gly261Asp
ENST00000262186.9:c.1802G>A	ENSP00000262186.5:p.Gly601Asp
ENST00000330883.8:c.782G>A	ENSP00000328531.4:p.Gly261Asp
ENST00000430723.4:c.1454G>A	ENSP00000387657.4:p.Gly485Asp
ENST00000461280.1:n.1089G>A
ENST00000473610.5:n.1107G>A
ENST00000532957.5:n.2025G>A
NM_000238.3:c.1802G>A , LRG_288t1:c.1802G>A	NP_000229.1:p.Gly601Asp
NM_001204798.1:c.782G>A	NP_001191727.1:p.Gly261Asp
NM_172056.2:c.1802G>A , LRG_288t2:c.1802G>A	NP_742053.1:p.Gly601Asp
NM_172057.2:c.782G>A , LRG_288t3:c.782G>A	NP_742054.1:p.Gly261Asp
XM_011516185.1:c.1502G>A	XP_011514487.1:p.Gly501Asp
XM_011516186.1:c.1802G>A	XP_011514488.1:p.Gly601Asp
XM_011516185.2:c.1502G>A	XP_011514487.1:p.Gly501Asp
XM_011516186.3:c.1802G>A	XP_011514488.1:p.Gly601Asp
XM_017012195.1:c.1652G>A	XP_016867684.1:p.Gly551Asp
XM_017012196.1:c.1625G>A	XP_016867685.1:p.Gly542Asp
NM_000238.4:c.1802G>A MANE Select	NP_000229.1:p.Gly601Asp
NM_001204798.2:c.782G>A	NP_001191727.1:p.Gly261Asp
NM_172057.3:c.782G>A	NP_742054.1:p.Gly261Asp