Canonical Allele Identifier: CA008740

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 67522
• ClinVar RCV Id: RCV000058251
• dbSNP Id: rs199472873
• MyVariant Identifiers: chr7:g.150655312G>C (hg19) ; chr7:g.150958224G>C (hg38)
• PubMed: PMID:14661677 ; PMID:19841300 ; PMID:22581653

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958224G>C , CM000669.2:g.150958224G>C	GRCh38
NC_000007.13:g.150655312G>C , CM000669.1:g.150655312G>C	GRCh37
NC_000007.12:g.150286245G>C	NCBI36
NG_008916.1:g.24703C>G , LRG_288:g.24703C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.1584C>G
ENST00000262186.10:c.751C>G MANE Select	ENSP00000262186.5:p.Pro251Ala
ENST00000262186.9:c.751C>G	ENSP00000262186.5:p.Pro251Ala
ENST00000430723.4:c.403C>G	ENSP00000387657.4:p.Pro135Ala
ENST00000532957.5:n.974C>G
NM_000238.3:c.751C>G , LRG_288t1:c.751C>G	NP_000229.1:p.Pro251Ala
NM_172056.2:c.751C>G , LRG_288t2:c.751C>G	NP_742053.1:p.Pro251Ala
XM_011516185.1:c.451C>G	XP_011514487.1:p.Pro151Ala
XM_011516186.1:c.751C>G	XP_011514488.1:p.Pro251Ala
XM_011516185.2:c.451C>G	XP_011514487.1:p.Pro151Ala
XM_011516186.3:c.751C>G	XP_011514488.1:p.Pro251Ala
XM_017012195.1:c.601C>G	XP_016867684.1:p.Pro201Ala
XM_017012196.1:c.574C>G	XP_016867685.1:p.Pro192Ala
NM_000238.4:c.751C>G MANE Select	NP_000229.1:p.Pro251Ala