Canonical Allele Identifier: CA369865829

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150671969T>A (hg19) ; chr7:g.150974881T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150974881T>A , CM000669.2:g.150974881T>A	GRCh38
NC_000007.13:g.150671969T>A , CM000669.1:g.150671969T>A	GRCh37
NC_000007.12:g.150302902T>A	NCBI36
NG_008916.1:g.8046A>T , LRG_288:g.8046A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262186.10:c.137A>T MANE Select	ENSP00000262186.5:p.Asp46Val
ENST00000262186.9:c.137A>T	ENSP00000262186.5:p.Asp46Val
ENST00000430723.4:c.-41A>T	ENSP00000387657.4:n.-41A>T
ENST00000532957.5:n.360A>T
NM_000238.3:c.137A>T , LRG_288t1:c.137A>T	NP_000229.1:p.Asp46Val
NM_172056.2:c.137A>T , LRG_288t2:c.137A>T	NP_742053.1:p.Asp46Val
XM_011516186.1:c.137A>T	XP_011514488.1:p.Asp46Val
XM_011516186.3:c.137A>T	XP_011514488.1:p.Asp46Val
XM_017012196.1:c.-41A>T	XP_016867685.1:n.-41A>T
NM_000238.4:c.137A>T MANE Select	NP_000229.1:p.Asp46Val