Canonical Allele Identifier: CA369861615

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150654476T>A (hg19) ; chr7:g.150957388T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150957388T>A , CM000669.2:g.150957388T>A	GRCh38
NC_000007.13:g.150654476T>A , CM000669.1:g.150654476T>A	GRCh37
NC_000007.12:g.150285409T>A	NCBI36
NG_008916.1:g.25539A>T , LRG_288:g.25539A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.1864A>T
ENST00000262186.10:c.1031A>T MANE Select	ENSP00000262186.5:p.Lys344Met
ENST00000262186.9:c.1031A>T	ENSP00000262186.5:p.Lys344Met
ENST00000430723.4:c.683A>T	ENSP00000387657.4:p.Lys228Met
ENST00000532957.5:n.1254A>T
NM_000238.3:c.1031A>T , LRG_288t1:c.1031A>T	NP_000229.1:p.Lys344Met
NM_172056.2:c.1031A>T , LRG_288t2:c.1031A>T	NP_742053.1:p.Lys344Met
XM_011516185.1:c.731A>T	XP_011514487.1:p.Lys244Met
XM_011516186.1:c.1031A>T	XP_011514488.1:p.Lys344Met
XM_011516185.2:c.731A>T	XP_011514487.1:p.Lys244Met
XM_011516186.3:c.1031A>T	XP_011514488.1:p.Lys344Met
XM_017012195.1:c.881A>T	XP_016867684.1:p.Lys294Met
XM_017012196.1:c.854A>T	XP_016867685.1:p.Lys285Met
NM_000238.4:c.1031A>T MANE Select	NP_000229.1:p.Lys344Met