Canonical Allele Identifier: CA369863685

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150656710G>C (hg19) ; chr7:g.150959622G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150959622G>C , CM000669.2:g.150959622G>C	GRCh38
NC_000007.13:g.150656710G>C , CM000669.1:g.150656710G>C	GRCh37
NC_000007.12:g.150287643G>C	NCBI36
NG_008916.1:g.23305C>G , LRG_288:g.23305C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1255C>G
ENST00000262186.10:c.422C>G MANE Select	ENSP00000262186.5:p.Pro141Arg
ENST00000262186.9:c.422C>G	ENSP00000262186.5:p.Pro141Arg
ENST00000430723.4:c.234+11C>G	ENSP00000387657.4:n.234+11C>G
ENST00000532957.5:n.645C>G
NM_000238.3:c.422C>G , LRG_288t1:c.422C>G	NP_000229.1:p.Pro141Arg
NM_172056.2:c.422C>G , LRG_288t2:c.422C>G	NP_742053.1:p.Pro141Arg
XM_011516185.1:c.122C>G	XP_011514487.1:p.Pro41Arg
XM_011516186.1:c.422C>G	XP_011514488.1:p.Pro141Arg
XM_011516185.2:c.122C>G	XP_011514487.1:p.Pro41Arg
XM_011516186.3:c.422C>G	XP_011514488.1:p.Pro141Arg
XM_017012195.1:c.272C>G	XP_016867684.1:p.Pro91Arg
XM_017012196.1:c.245C>G	XP_016867685.1:p.Pro82Arg
NM_000238.4:c.422C>G MANE Select	NP_000229.1:p.Pro141Arg