Canonical Allele Identifier: CA344876342

Gene: KCNH1

Linked Data

• MyVariant Identifiers: chr1:g.211192493A>T (hg19) ; chr1:g.211019151A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.211019151A>T , CM000663.2:g.211019151A>T	GRCh38
NC_000001.10:g.211192493A>T , CM000663.1:g.211192493A>T	GRCh37
NC_000001.9:g.209259116A>T	NCBI36
NG_029777.1:g.119965T>A
NG_029777.2:g.119965T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271751.10:c.664T>A MANE Select	ENSP00000271751.4:p.Trp222Arg
ENST00000367007.5:c.664T>A	ENSP00000355974.5:p.Trp222Arg
ENST00000638357.1:c.78T>A
ENST00000638498.1:c.664T>A	ENSP00000490983.1:p.Trp222Arg
ENST00000638960.1:c.664T>A	ENSP00000492302.1:p.Trp222Arg
ENST00000638983.1:c.664T>A	ENSP00000492641.1:p.Trp222Arg
ENST00000639385.1:n.40T>A
ENST00000639602.1:c.535T>A	ENSP00000492303.1:p.Trp179Arg
ENST00000639754.1:n.867T>A
ENST00000639952.1:c.664T>A	ENSP00000492697.1:p.Trp222Arg
ENST00000640044.1:c.310+84345T>A	ENSP00000491434.1:n.310+84345T>A
ENST00000640243.1:c.664T>A	ENSP00000492803.1:p.Trp222Arg
ENST00000640522.1:c.664T>A	ENSP00000491019.1:p.Trp222Arg
ENST00000640528.1:c.664T>A	ENSP00000491725.1:p.Trp222Arg
ENST00000640566.1:c.310+84345T>A	ENSP00000491302.1:n.310+84345T>A
ENST00000640710.1:c.664T>A	ENSP00000492513.1:p.Trp222Arg
ENST00000640890.1:n.766T>A
ENST00000271751.8:c.664T>A	ENSP00000271751.4:p.Trp222Arg
ENST00000367007.4:c.664T>A	ENSP00000355974.4:p.Trp222Arg
NM_002238.3:c.664T>A	NP_002229.1:p.Trp222Arg
NM_172362.2:c.664T>A	NP_758872.1:p.Trp222Arg
NM_172362.3:c.664T>A MANE Select	NP_758872.1:p.Trp222Arg
NM_002238.4:c.664T>A	NP_002229.1:p.Trp222Arg