Canonical Allele Identifier: CA369860271

Gene: KCNH2

Linked Data

• dbSNP Id: rs769814960
• gnomAD v3: 7-150952804-G-C
• gnomAD v4: 7-150952804-G-C
• MyVariant Identifiers: chr7:g.150649892G>C (hg19) ; chr7:g.150952804G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952804G>C , CM000669.2:g.150952804G>C	GRCh38
NC_000007.13:g.150649892G>C , CM000669.1:g.150649892G>C	GRCh37
NC_000007.12:g.150280825G>C	NCBI36
NG_008916.1:g.30123C>G , LRG_288:g.30123C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.476C>G
ENST00000684116.1:n.71C>G
ENST00000684241.1:n.2011C>G
ENST00000262186.10:c.1178C>G MANE Select	ENSP00000262186.5:p.Pro393Arg
ENST00000330883.9:c.158C>G	ENSP00000328531.4:p.Pro53Arg
ENST00000262186.9:c.1178C>G	ENSP00000262186.5:p.Pro393Arg
ENST00000330883.8:c.158C>G	ENSP00000328531.4:p.Pro53Arg
ENST00000430723.4:c.830C>G	ENSP00000387657.4:p.Pro277Arg
ENST00000461280.1:n.465C>G
ENST00000473610.5:n.483C>G
ENST00000532957.5:n.1401C>G
NM_000238.3:c.1178C>G , LRG_288t1:c.1178C>G	NP_000229.1:p.Pro393Arg
NM_001204798.1:c.158C>G	NP_001191727.1:p.Pro53Arg
NM_172056.2:c.1178C>G , LRG_288t2:c.1178C>G	NP_742053.1:p.Pro393Arg
NM_172057.2:c.158C>G , LRG_288t3:c.158C>G	NP_742054.1:p.Pro53Arg
XM_011516185.1:c.878C>G	XP_011514487.1:p.Pro293Arg
XM_011516186.1:c.1178C>G	XP_011514488.1:p.Pro393Arg
XM_011516185.2:c.878C>G	XP_011514487.1:p.Pro293Arg
XM_011516186.3:c.1178C>G	XP_011514488.1:p.Pro393Arg
XM_017012195.1:c.1028C>G	XP_016867684.1:p.Pro343Arg
XM_017012196.1:c.1001C>G	XP_016867685.1:p.Pro334Arg
NM_000238.4:c.1178C>G MANE Select	NP_000229.1:p.Pro393Arg
NM_001204798.2:c.158C>G	NP_001191727.1:p.Pro53Arg
NM_172057.3:c.158C>G	NP_742054.1:p.Pro53Arg