Canonical Allele Identifier: CA369856600

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150647461G>C (hg19) ; chr7:g.150950373G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150950373G>C , CM000669.2:g.150950373G>C	GRCh38
NC_000007.13:g.150647461G>C , CM000669.1:g.150647461G>C	GRCh37
NC_000007.12:g.150278394G>C	NCBI36
NG_008916.1:g.32554C>G , LRG_288:g.32554C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1491C>G
ENST00000684241.1:n.3026C>G
ENST00000262186.10:c.2193C>G MANE Select	ENSP00000262186.5:p.His731Gln
ENST00000330883.9:c.1173C>G	ENSP00000328531.4:p.His391Gln
ENST00000262186.9:c.2193C>G	ENSP00000262186.5:p.His731Gln
ENST00000330883.8:c.1173C>G	ENSP00000328531.4:p.His391Gln
ENST00000430723.4:c.1845C>G	ENSP00000387657.4:p.His615Gln
ENST00000461280.1:n.1480C>G
ENST00000473610.5:n.1825C>G
ENST00000532957.5:n.2416C>G
NM_000238.3:c.2193C>G , LRG_288t1:c.2193C>G	NP_000229.1:p.His731Gln
NM_001204798.1:c.1173C>G	NP_001191727.1:p.His391Gln
NM_172056.2:c.2193C>G , LRG_288t2:c.2193C>G	NP_742053.1:p.His731Gln
NM_172057.2:c.1173C>G , LRG_288t3:c.1173C>G	NP_742054.1:p.His391Gln
XM_011516185.1:c.1893C>G	XP_011514487.1:p.His631Gln
XM_011516186.1:c.2193C>G	XP_011514488.1:p.His731Gln
XM_011516185.2:c.1893C>G	XP_011514487.1:p.His631Gln
XM_011516186.3:c.2193C>G	XP_011514488.1:p.His731Gln
XM_017012195.1:c.2043C>G	XP_016867684.1:p.His681Gln
XM_017012196.1:c.2016C>G	XP_016867685.1:p.His672Gln
NM_000238.4:c.2193C>G MANE Select	NP_000229.1:p.His731Gln
NM_001204798.2:c.1173C>G	NP_001191727.1:p.His391Gln
NM_172057.3:c.1173C>G	NP_742054.1:p.His391Gln