Canonical Allele Identifier: CA1752430486

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947846C= , CM000669.2:g.150947846C=	GRCh38
NC_000007.13:g.150644934C= , CM000669.1:g.150644934C=	GRCh37
NC_000007.12:g.150275867C=	NCBI36
NG_008916.1:g.35081G= , LRG_288:g.35081G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3558G=
ENST00000262186.10:c.2725G= MANE Select	ENSP00000262186.5:p.Gly909=
ENST00000330883.9:c.1705G=	ENSP00000328531.4:p.Gly569=
ENST00000262186.9:c.2725G=	ENSP00000262186.5:p.Gly909=
ENST00000330883.8:c.1705G=	ENSP00000328531.4:p.Gly569=
NM_000238.3:c.2725G= , LRG_288t1:c.2725G=	NP_000229.1:p.Gly909=
NM_172057.2:c.1705G= , LRG_288t3:c.1705G=	NP_742054.1:p.Gly569=
XM_011516185.1:c.2425G=	XP_011514487.1:p.Gly809=
XM_011516186.1:c.2693-155G=	XP_011514488.1:n.2693-155G=
XM_011516185.2:c.2425G=	XP_011514487.1:p.Gly809=
XM_011516186.3:c.2693-155G=	XP_011514488.1:n.2693-155G=
XM_017012195.1:c.2575G=	XP_016867684.1:p.Gly859=
XM_017012196.1:c.2548G=	XP_016867685.1:p.Gly850=
NM_000238.4:c.2725G= MANE Select	NP_000229.1:p.Gly909=
NM_172057.3:c.1705G=	NP_742054.1:p.Gly569=