Canonical Allele Identifier: CA1752429936

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150947665C= , CM000669.2:g.150947665C=	GRCh38
NC_000007.13:g.150644753C= , CM000669.1:g.150644753C=	GRCh37
NC_000007.12:g.150275686C=	NCBI36
NG_008916.1:g.35262G= , LRG_288:g.35262G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.3739G=
ENST00000262186.10:c.2906G= MANE Select	ENSP00000262186.5:p.Gly969=
ENST00000330883.9:c.1886G=	ENSP00000328531.4:p.Gly629=
ENST00000262186.9:c.2906G=	ENSP00000262186.5:p.Gly969=
ENST00000330883.8:c.1886G=	ENSP00000328531.4:p.Gly629=
NM_000238.3:c.2906G= , LRG_288t1:c.2906G=	NP_000229.1:p.Gly969=
NM_172057.2:c.1886G= , LRG_288t3:c.1886G=	NP_742054.1:p.Gly629=
XM_011516185.1:c.2606G=	XP_011514487.1:p.Gly869=
XM_011516186.1:c.2719G=	XP_011514488.1:p.Val907=
XM_011516185.2:c.2606G=	XP_011514487.1:p.Gly869=
XM_011516186.3:c.2719G=	XP_011514488.1:p.Val907=
XM_017012195.1:c.2756G=	XP_016867684.1:p.Gly919=
XM_017012196.1:c.2729G=	XP_016867685.1:p.Gly910=
NM_000238.4:c.2906G= MANE Select	NP_000229.1:p.Gly969=
NM_172057.3:c.1886G=	NP_742054.1:p.Gly629=