Canonical Allele Identifier: CA369862545

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150655290G>C (hg19) ; chr7:g.150958202G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958202G>C , CM000669.2:g.150958202G>C	GRCh38
NC_000007.13:g.150655290G>C , CM000669.1:g.150655290G>C	GRCh37
NC_000007.12:g.150286223G>C	NCBI36
NG_008916.1:g.24725C>G , LRG_288:g.24725C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.1606C>G
ENST00000262186.10:c.773C>G MANE Select	ENSP00000262186.5:p.Pro258Arg
ENST00000262186.9:c.773C>G	ENSP00000262186.5:p.Pro258Arg
ENST00000430723.4:c.425C>G	ENSP00000387657.4:p.Pro142Arg
ENST00000532957.5:n.996C>G
NM_000238.3:c.773C>G , LRG_288t1:c.773C>G	NP_000229.1:p.Pro258Arg
NM_172056.2:c.773C>G , LRG_288t2:c.773C>G	NP_742053.1:p.Pro258Arg
XM_011516185.1:c.473C>G	XP_011514487.1:p.Pro158Arg
XM_011516186.1:c.773C>G	XP_011514488.1:p.Pro258Arg
XM_011516185.2:c.473C>G	XP_011514487.1:p.Pro158Arg
XM_011516186.3:c.773C>G	XP_011514488.1:p.Pro258Arg
XM_017012195.1:c.623C>G	XP_016867684.1:p.Pro208Arg
XM_017012196.1:c.596C>G	XP_016867685.1:p.Pro199Arg
NM_000238.4:c.773C>G MANE Select	NP_000229.1:p.Pro258Arg