Canonical Allele Identifier: CA37111546

Gene: KCNH1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.210683457C>T , CM000663.2:g.210683457C>T	GRCh38
NC_000001.10:g.210856799C>T , CM000663.1:g.210856799C>T	GRCh37
NC_000001.9:g.208923422C>T	NCBI36
NG_029777.1:g.455659G>A
NG_029777.2:g.455659G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271751.10:c.2794G>A MANE Select	ENSP00000271751.4:p.Glu932Lys
ENST00000367007.5:c.2703+10G>A	ENSP00000355974.5:n.2703+10G>A
ENST00000638357.1:c.1930G>A
ENST00000638498.1:c.2784+10G>A	ENSP00000490983.1:n.2784+10G>A
ENST00000638960.1:c.2713G>A	ENSP00000492302.1:p.Glu905Lys
ENST00000639952.1:c.2713G>A	ENSP00000492697.1:p.Glu905Lys
ENST00000640044.1:c.1642G>A	ENSP00000491434.1:p.Glu548Lys
ENST00000640243.1:c.*1299G>A	ENSP00000492803.1:n.*1299G>A
ENST00000640528.1:c.2713G>A	ENSP00000491725.1:p.Glu905Lys
ENST00000640566.1:c.1189G>A	ENSP00000491302.1:p.Glu397Lys
ENST00000640625.1:c.463+10G>A
ENST00000640710.1:c.2713G>A	ENSP00000492513.1:p.Glu905Lys
ENST00000271751.8:c.2794G>A	ENSP00000271751.4:p.Glu932Lys
ENST00000367007.4:c.2713G>A	ENSP00000355974.4:p.Glu905Lys
NM_002238.3:c.2713G>A	NP_002229.1:p.Glu905Lys
NM_172362.2:c.2794G>A	NP_758872.1:p.Glu932Lys
XM_011509514.1:c.1618G>A	XP_011507816.1:p.Glu540Lys
XM_017001246.1:c.1618G>A	XP_016856735.1:p.Glu540Lys
NM_172362.3:c.2794G>A MANE Select	NP_758872.1:p.Glu932Lys
NM_002238.4:c.2713G>A	NP_002229.1:p.Glu905Lys