Canonical Allele Identifier: CA1752431546

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948542G= , CM000669.2:g.150948542G=	GRCh38
NC_000007.13:g.150645630G= , CM000669.1:g.150645630G=	GRCh37
NC_000007.12:g.150276563G=	NCBI36
NG_008916.1:g.34385C= , LRG_288:g.34385C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3427C=
ENST00000262186.10:c.2594C= MANE Select	ENSP00000262186.5:p.Thr865=
ENST00000330883.9:c.1574C=	ENSP00000328531.4:p.Thr525=
ENST00000262186.9:c.2594C=	ENSP00000262186.5:p.Thr865=
ENST00000330883.8:c.1574C=	ENSP00000328531.4:p.Thr525=
NM_000238.3:c.2594C= , LRG_288t1:c.2594C=	NP_000229.1:p.Thr865=
NM_172057.2:c.1574C= , LRG_288t3:c.1574C=	NP_742054.1:p.Thr525=
XM_011516185.1:c.2294C=	XP_011514487.1:p.Thr765=
XM_011516186.1:c.2594C=	XP_011514488.1:p.Thr865=
XM_011516185.2:c.2294C=	XP_011514487.1:p.Thr765=
XM_011516186.3:c.2594C=	XP_011514488.1:p.Thr865=
XM_017012195.1:c.2444C=	XP_016867684.1:p.Thr815=
XM_017012196.1:c.2417C=	XP_016867685.1:p.Thr806=
NM_000238.4:c.2594C= MANE Select	NP_000229.1:p.Thr865=
NM_172057.3:c.1574C=	NP_742054.1:p.Thr525=