Canonical Allele Identifier: CA1752414986

Gene: KCNH2

Linked Data

• dbSNP Id: rs1801346214
• gnomAD v4: 7-150955668-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150955668C>T , CM000669.2:g.150955668C>T	GRCh38
NC_000007.13:g.150652756C>T , CM000669.1:g.150652756C>T	GRCh37
NC_000007.12:g.150283689C>T	NCBI36
NG_008916.1:g.27259G>A , LRG_288:g.27259G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.154G>A
ENST00000684241.1:n.1961+1623G>A
ENST00000262186.10:c.1128+1623G>A MANE Select	ENSP00000262186.5:n.1128+1623G>A
ENST00000330883.9:c.-165G>A	ENSP00000328531.4:n.-165G>A
ENST00000262186.9:c.1128+1623G>A	ENSP00000262186.5:n.1128+1623G>A
ENST00000330883.8:c.-165G>A	ENSP00000328531.4:n.-165G>A
ENST00000430723.4:c.780+1623G>A	ENSP00000387657.4:n.780+1623G>A
ENST00000461280.1:n.143G>A
ENST00000473610.5:n.161G>A
ENST00000532957.5:n.1351+1623G>A
NM_000238.3:c.1128+1623G>A , LRG_288t1:c.1128+1623G>A	NP_000229.1:n.1128+1623G>A
NM_001204798.1:c.-165G>A	NP_001191727.1:n.-165G>A
NM_172056.2:c.1128+1623G>A , LRG_288t2:c.1128+1623G>A	NP_742053.1:n.1128+1623G>A
NM_172057.2:c.-165G>A , LRG_288t3:c.-165G>A	NP_742054.1:n.-165G>A
XM_011516185.1:c.828+1623G>A	XP_011514487.1:n.828+1623G>A
XM_011516186.1:c.1128+1623G>A	XP_011514488.1:n.1128+1623G>A
XM_011516185.2:c.828+1623G>A	XP_011514487.1:n.828+1623G>A
XM_011516186.3:c.1128+1623G>A	XP_011514488.1:n.1128+1623G>A
XM_017012195.1:c.978+1623G>A	XP_016867684.1:n.978+1623G>A
XM_017012196.1:c.951+1623G>A	XP_016867685.1:n.951+1623G>A
NM_000238.4:c.1128+1623G>A MANE Select	NP_000229.1:n.1128+1623G>A
NM_001204798.2:c.-165G>A	NP_001191727.1:n.-165G>A
NM_172057.3:c.-165G>A	NP_742054.1:n.-165G>A