Canonical Allele Identifier: CA369854730

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150645962G>C (hg19) ; chr7:g.150948874G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948874G>C , CM000669.2:g.150948874G>C	GRCh38
NC_000007.13:g.150645962G>C , CM000669.1:g.150645962G>C	GRCh37
NC_000007.12:g.150276895G>C	NCBI36
NG_008916.1:g.34053C>G , LRG_288:g.34053C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3407C>G
ENST00000262186.10:c.2574C>G MANE Select	ENSP00000262186.5:p.Ile858Met
ENST00000330883.9:c.1554C>G	ENSP00000328531.4:p.Ile518Met
ENST00000262186.9:c.2574C>G	ENSP00000262186.5:p.Ile858Met
ENST00000330883.8:c.1554C>G	ENSP00000328531.4:p.Ile518Met
NM_000238.3:c.2574C>G , LRG_288t1:c.2574C>G	NP_000229.1:p.Ile858Met
NM_172057.2:c.1554C>G , LRG_288t3:c.1554C>G	NP_742054.1:p.Ile518Met
XM_011516185.1:c.2274C>G	XP_011514487.1:p.Ile758Met
XM_011516186.1:c.2574C>G	XP_011514488.1:p.Ile858Met
XM_011516185.2:c.2274C>G	XP_011514487.1:p.Ile758Met
XM_011516186.3:c.2574C>G	XP_011514488.1:p.Ile858Met
XM_017012195.1:c.2424C>G	XP_016867684.1:p.Ile808Met
XM_017012196.1:c.2397C>G	XP_016867685.1:p.Ile799Met
NM_000238.4:c.2574C>G MANE Select	NP_000229.1:p.Ile858Met
NM_172057.3:c.1554C>G	NP_742054.1:p.Ile518Met