Canonical Allele Identifier: CA369861543

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150654442G>T (hg19) ; chr7:g.150957354G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150957354G>T , CM000669.2:g.150957354G>T	GRCh38
NC_000007.13:g.150654442G>T , CM000669.1:g.150654442G>T	GRCh37
NC_000007.12:g.150285375G>T	NCBI36
NG_008916.1:g.25573C>A , LRG_288:g.25573C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1898C>A
ENST00000262186.10:c.1065C>A MANE Select	ENSP00000262186.5:p.Asp355Glu
ENST00000262186.9:c.1065C>A	ENSP00000262186.5:p.Asp355Glu
ENST00000430723.4:c.717C>A	ENSP00000387657.4:p.Asp239Glu
ENST00000532957.5:n.1288C>A
NM_000238.3:c.1065C>A , LRG_288t1:c.1065C>A	NP_000229.1:p.Asp355Glu
NM_172056.2:c.1065C>A , LRG_288t2:c.1065C>A	NP_742053.1:p.Asp355Glu
XM_011516185.1:c.765C>A	XP_011514487.1:p.Asp255Glu
XM_011516186.1:c.1065C>A	XP_011514488.1:p.Asp355Glu
XM_011516185.2:c.765C>A	XP_011514487.1:p.Asp255Glu
XM_011516186.3:c.1065C>A	XP_011514488.1:p.Asp355Glu
XM_017012195.1:c.915C>A	XP_016867684.1:p.Asp305Glu
XM_017012196.1:c.888C>A	XP_016867685.1:p.Asp296Glu
NM_000238.4:c.1065C>A MANE Select	NP_000229.1:p.Asp355Glu