Canonical Allele Identifier: CA369854791

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948889C>T , CM000669.2:g.150948889C>T	GRCh38
NC_000007.13:g.150645977C>T , CM000669.1:g.150645977C>T	GRCh37
NC_000007.12:g.150276910C>T	NCBI36
NG_008916.1:g.34038G>A , LRG_288:g.34038G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000238.4:c.2559G>A MANE Select	NP_000229.1:p.Trp853Ter
ENST00000262186.10:c.2559G>A MANE Select	ENSP00000262186.5:p.Trp853Ter
NM_000238.3:c.2559G>A , LRG_288t1:c.2559G>A	NP_000229.1:p.Trp853Ter
NM_172057.2:c.1539G>A , LRG_288t3:c.1539G>A	NP_742054.1:p.Trp513Ter
NM_172057.3:c.1539G>A	NP_742054.1:p.Trp513Ter
ENST00000262186.9:c.2559G>A	ENSP00000262186.5:p.Trp853Ter
ENST00000330883.8:c.1539G>A	ENSP00000328531.4:p.Trp513Ter
ENST00000330883.9:c.1539G>A	ENSP00000328531.4:p.Trp513Ter
ENST00000684241.1:n.3392G>A
XM_011516185.1:c.2259G>A	XP_011514487.1:p.Trp753Ter
XM_011516185.2:c.2259G>A	XP_011514487.1:p.Trp753Ter
XM_011516186.1:c.2559G>A	XP_011514488.1:p.Trp853Ter
XM_011516186.3:c.2559G>A	XP_011514488.1:p.Trp853Ter
XM_017012195.1:c.2409G>A	XP_016867684.1:p.Trp803Ter
XM_017012196.1:c.2382G>A	XP_016867685.1:p.Trp794Ter