Canonical Allele Identifier: CA1752411986

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952662C= , CM000669.2:g.150952662C=	GRCh38
NC_000007.13:g.150649750C= , CM000669.1:g.150649750C=	GRCh37
NC_000007.12:g.150280683C=	NCBI36
NG_008916.1:g.30265G= , LRG_288:g.30265G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.618G=
ENST00000684116.1:n.213G=
ENST00000684241.1:n.2153G=
ENST00000262186.10:c.1320G= MANE Select	ENSP00000262186.5:p.Pro440=
ENST00000330883.9:c.300G=	ENSP00000328531.4:p.Pro100=
ENST00000262186.9:c.1320G=	ENSP00000262186.5:p.Pro440=
ENST00000330883.8:c.300G=	ENSP00000328531.4:p.Pro100=
ENST00000430723.4:c.972G=	ENSP00000387657.4:p.Pro324=
ENST00000461280.1:n.607G=
ENST00000473610.5:n.625G=
ENST00000532957.5:n.1543G=
NM_000238.3:c.1320G= , LRG_288t1:c.1320G=	NP_000229.1:p.Pro440=
NM_001204798.1:c.300G=	NP_001191727.1:p.Pro100=
NM_172056.2:c.1320G= , LRG_288t2:c.1320G=	NP_742053.1:p.Pro440=
NM_172057.2:c.300G= , LRG_288t3:c.300G=	NP_742054.1:p.Pro100=
XM_011516185.1:c.1020G=	XP_011514487.1:p.Pro340=
XM_011516186.1:c.1320G=	XP_011514488.1:p.Pro440=
XM_011516185.2:c.1020G=	XP_011514487.1:p.Pro340=
XM_011516186.3:c.1320G=	XP_011514488.1:p.Pro440=
XM_017012195.1:c.1170G=	XP_016867684.1:p.Pro390=
XM_017012196.1:c.1143G=	XP_016867685.1:p.Pro381=
NM_000238.4:c.1320G= MANE Select	NP_000229.1:p.Pro440=
NM_001204798.2:c.300G=	NP_001191727.1:p.Pro100=
NM_172057.3:c.300G=	NP_742054.1:p.Pro100=