Canonical Allele Identifier: CA369863760

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150656743T>A (hg19) ; chr7:g.150959655T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150959655T>A , CM000669.2:g.150959655T>A	GRCh38
NC_000007.13:g.150656743T>A , CM000669.1:g.150656743T>A	GRCh37
NC_000007.12:g.150287676T>A	NCBI36
NG_008916.1:g.23272A>T , LRG_288:g.23272A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1222A>T
ENST00000262186.10:c.389A>T MANE Select	ENSP00000262186.5:p.Glu130Val
ENST00000262186.9:c.389A>T	ENSP00000262186.5:p.Glu130Val
ENST00000430723.4:c.212A>T	ENSP00000387657.4:p.Glu71Val
ENST00000532957.5:n.612A>T
NM_000238.3:c.389A>T , LRG_288t1:c.389A>T	NP_000229.1:p.Glu130Val
NM_172056.2:c.389A>T , LRG_288t2:c.389A>T	NP_742053.1:p.Glu130Val
XM_011516185.1:c.89A>T	XP_011514487.1:p.Glu30Val
XM_011516186.1:c.389A>T	XP_011514488.1:p.Glu130Val
XM_011516185.2:c.89A>T	XP_011514487.1:p.Glu30Val
XM_011516186.3:c.389A>T	XP_011514488.1:p.Glu130Val
XM_017012195.1:c.239A>T	XP_016867684.1:p.Glu80Val
XM_017012196.1:c.212A>T	XP_016867685.1:p.Glu71Val
NM_000238.4:c.389A>T MANE Select	NP_000229.1:p.Glu130Val