Canonical Allele Identifier: CA423146025
Gene: KCNH1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.211192428G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.211019086G>T , CM000663.2:g.211019086G>T GRCh38
NC_000001.10:g.211192428G>T , CM000663.1:g.211192428G>T GRCh37
NC_000001.9:g.209259051G>T NCBI36
NG_029777.1:g.120030C>A
NG_029777.2:g.120030C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000271751.10:c.729C>A MANE Select ENSP00000271751.4:p.Thr243=
ENST00000367007.5:c.729C>A ENSP00000355974.5:p.Thr243=
ENST00000638357.1:c.143C>A
ENST00000638498.1:c.729C>A ENSP00000490983.1:p.Thr243=
ENST00000638960.1:c.729C>A ENSP00000492302.1:p.Thr243=
ENST00000638983.1:c.729C>A ENSP00000492641.1:p.Thr243=
ENST00000639385.1:n.105C>A
ENST00000639602.1:c.600C>A ENSP00000492303.1:p.Thr200=
ENST00000639754.1:n.932C>A
ENST00000639952.1:c.729C>A ENSP00000492697.1:p.Thr243=
ENST00000640044.1:c.310+84410C>A ENSP00000491434.1:n.310+84410C>A
ENST00000640243.1:c.729C>A ENSP00000492803.1:p.Thr243=
ENST00000640522.1:c.729C>A ENSP00000491019.1:p.Thr243=
ENST00000640528.1:c.729C>A ENSP00000491725.1:p.Thr243=
ENST00000640566.1:c.310+84410C>A ENSP00000491302.1:n.310+84410C>A
ENST00000640710.1:c.729C>A ENSP00000492513.1:p.Thr243=
ENST00000640890.1:n.831C>A
ENST00000271751.8:c.729C>A ENSP00000271751.4:p.Thr243=
ENST00000367007.4:c.729C>A ENSP00000355974.4:p.Thr243=
NM_002238.3:c.729C>A NP_002229.1:p.Thr243=
NM_172362.2:c.729C>A NP_758872.1:p.Thr243=
NM_172362.3:c.729C>A MANE Select NP_758872.1:p.Thr243=
NM_002238.4:c.729C>A NP_002229.1:p.Thr243=