Canonical Allele Identifier: CA369853669

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150645553A>T (hg19) ; chr7:g.150948465A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948465A>T , CM000669.2:g.150948465A>T	GRCh38
NC_000007.13:g.150645553A>T , CM000669.1:g.150645553A>T	GRCh37
NC_000007.12:g.150276486A>T	NCBI36
NG_008916.1:g.34462T>A , LRG_288:g.34462T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3504T>A
ENST00000262186.10:c.2671T>A MANE Select	ENSP00000262186.5:p.Phe891Ile
ENST00000330883.9:c.1651T>A	ENSP00000328531.4:p.Phe551Ile
ENST00000262186.9:c.2671T>A	ENSP00000262186.5:p.Phe891Ile
ENST00000330883.8:c.1651T>A	ENSP00000328531.4:p.Phe551Ile
NM_000238.3:c.2671T>A , LRG_288t1:c.2671T>A	NP_000229.1:p.Phe891Ile
NM_172057.2:c.1651T>A , LRG_288t3:c.1651T>A	NP_742054.1:p.Phe551Ile
XM_011516185.1:c.2371T>A	XP_011514487.1:p.Phe791Ile
XM_011516186.1:c.2671T>A	XP_011514488.1:p.Phe891Ile
XM_011516185.2:c.2371T>A	XP_011514487.1:p.Phe791Ile
XM_011516186.3:c.2671T>A	XP_011514488.1:p.Phe891Ile
XM_017012195.1:c.2521T>A	XP_016867684.1:p.Phe841Ile
XM_017012196.1:c.2494T>A	XP_016867685.1:p.Phe832Ile
NM_000238.4:c.2671T>A MANE Select	NP_000229.1:p.Phe891Ile
NM_172057.3:c.1651T>A	NP_742054.1:p.Phe551Ile