Canonical Allele Identifier: CA2484836186

Gene: KCNH1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.210920007G= , CM000663.2:g.210920007G=	GRCh38
NC_000001.10:g.211093349G= , CM000663.1:g.211093349G=	GRCh37
NC_000001.9:g.209159972G=	NCBI36
NG_029777.1:g.219109C=
NG_029777.2:g.219109C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271751.10:c.1095C= MANE Select	ENSP00000271751.4:p.Ala365=
ENST00000367007.5:c.1014C=	ENSP00000355974.5:p.Ala338=
ENST00000638357.1:c.428C=
ENST00000638498.1:c.1095C=	ENSP00000490983.1:p.Ala365=
ENST00000638960.1:c.1014C=	ENSP00000492302.1:p.Ala338=
ENST00000638983.1:c.952-58813C=	ENSP00000492641.1:n.952-58813C=
ENST00000639385.1:n.463C=
ENST00000639602.1:c.885C=	ENSP00000492303.1:p.Ala295=
ENST00000639754.1:n.1298C=
ENST00000639952.1:c.1014C=	ENSP00000492697.1:p.Ala338=
ENST00000640044.1:c.311-115841C=	ENSP00000491434.1:n.311-115841C=
ENST00000640243.1:c.951+98857C=	ENSP00000492803.1:n.951+98857C=
ENST00000640522.1:c.1032+98776C=	ENSP00000491019.1:n.1032+98776C=
ENST00000640528.1:c.1014C=	ENSP00000491725.1:p.Ala338=
ENST00000640566.1:c.311-144463C=	ENSP00000491302.1:n.311-144463C=
ENST00000640710.1:c.1014C=	ENSP00000492513.1:p.Ala338=
ENST00000640890.1:n.1116C=
ENST00000271751.8:c.1095C=	ENSP00000271751.4:p.Ala365=
ENST00000367007.4:c.1014C=	ENSP00000355974.4:p.Ala338=
NM_002238.3:c.1014C=	NP_002229.1:p.Ala338=
NM_172362.2:c.1095C=	NP_758872.1:p.Ala365=
XM_011509514.1:c.-82C=	XP_011507816.1:n.-82C=
XM_017001246.1:c.-82C=	XP_016856735.1:n.-82C=
NM_172362.3:c.1095C= MANE Select	NP_758872.1:p.Ala365=
NM_002238.4:c.1014C=	NP_002229.1:p.Ala338=