Canonical Allele Identifier: CA2484836182

Gene: KCNH1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.210919997C= , CM000663.2:g.210919997C=	GRCh38
NC_000001.10:g.211093339C= , CM000663.1:g.211093339C=	GRCh37
NC_000001.9:g.209159962C=	NCBI36
NG_029777.1:g.219119G=
NG_029777.2:g.219119G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271751.10:c.1105G= MANE Select	ENSP00000271751.4:p.Asp369=
ENST00000367007.5:c.1024G=	ENSP00000355974.5:p.Asp342=
ENST00000638357.1:c.438G=
ENST00000638498.1:c.1105G=	ENSP00000490983.1:p.Asp369=
ENST00000638960.1:c.1024G=	ENSP00000492302.1:p.Asp342=
ENST00000638983.1:c.952-58803G=	ENSP00000492641.1:n.952-58803G=
ENST00000639385.1:n.473G=
ENST00000639602.1:c.895G=	ENSP00000492303.1:p.Asp299=
ENST00000639754.1:n.1308G=
ENST00000639952.1:c.1024G=	ENSP00000492697.1:p.Asp342=
ENST00000640044.1:c.311-115831G=	ENSP00000491434.1:n.311-115831G=
ENST00000640243.1:c.951+98867G=	ENSP00000492803.1:n.951+98867G=
ENST00000640522.1:c.1032+98786G=	ENSP00000491019.1:n.1032+98786G=
ENST00000640528.1:c.1024G=	ENSP00000491725.1:p.Asp342=
ENST00000640566.1:c.311-144453G=	ENSP00000491302.1:n.311-144453G=
ENST00000640710.1:c.1024G=	ENSP00000492513.1:p.Asp342=
ENST00000640890.1:n.1126G=
ENST00000271751.8:c.1105G=	ENSP00000271751.4:p.Asp369=
ENST00000367007.4:c.1024G=	ENSP00000355974.4:p.Asp342=
NM_002238.3:c.1024G=	NP_002229.1:p.Asp342=
NM_172362.2:c.1105G=	NP_758872.1:p.Asp369=
XM_011509514.1:c.-72G=	XP_011507816.1:n.-72G=
XM_017001246.1:c.-72G=	XP_016856735.1:n.-72G=
NM_172362.3:c.1105G= MANE Select	NP_758872.1:p.Asp369=
NM_002238.4:c.1024G=	NP_002229.1:p.Asp342=