Canonical Allele Identifier: CA1752416769

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150957403T= , CM000669.2:g.150957403T=	GRCh38
NC_000007.13:g.150654491T= , CM000669.1:g.150654491T=	GRCh37
NC_000007.12:g.150285424T=	NCBI36
NG_008916.1:g.25524A= , LRG_288:g.25524A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1849A=
ENST00000262186.10:c.1016A= MANE Select	ENSP00000262186.5:p.Asn339=
ENST00000262186.9:c.1016A=	ENSP00000262186.5:p.Asn339=
ENST00000430723.4:c.668A=	ENSP00000387657.4:p.Asn223=
ENST00000532957.5:n.1239A=
NM_000238.3:c.1016A= , LRG_288t1:c.1016A=	NP_000229.1:p.Asn339=
NM_172056.2:c.1016A= , LRG_288t2:c.1016A=	NP_742053.1:p.Asn339=
XM_011516185.1:c.716A=	XP_011514487.1:p.Asn239=
XM_011516186.1:c.1016A=	XP_011514488.1:p.Asn339=
XM_011516185.2:c.716A=	XP_011514487.1:p.Asn239=
XM_011516186.3:c.1016A=	XP_011514488.1:p.Asn339=
XM_017012195.1:c.866A=	XP_016867684.1:p.Asn289=
XM_017012196.1:c.839A=	XP_016867685.1:p.Asn280=
NM_000238.4:c.1016A= MANE Select	NP_000229.1:p.Asn339=