Canonical Allele Identifier: CA423146017

Gene: KCNH1

Linked Data

• gnomAD v4: 1-211019083-C-T
• MyVariant Identifiers: chr1:g.211192425C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.211019083C>T , CM000663.2:g.211019083C>T	GRCh38
NC_000001.10:g.211192425C>T , CM000663.1:g.211192425C>T	GRCh37
NC_000001.9:g.209259048C>T	NCBI36
NG_029777.1:g.120033G>A
NG_029777.2:g.120033G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271751.10:c.732G>A MANE Select	ENSP00000271751.4:p.Arg244=
ENST00000367007.5:c.732G>A	ENSP00000355974.5:p.Arg244=
ENST00000638357.1:c.146G>A
ENST00000638498.1:c.732G>A	ENSP00000490983.1:p.Arg244=
ENST00000638960.1:c.732G>A	ENSP00000492302.1:p.Arg244=
ENST00000638983.1:c.732G>A	ENSP00000492641.1:p.Arg244=
ENST00000639385.1:n.108G>A
ENST00000639602.1:c.603G>A	ENSP00000492303.1:p.Arg201=
ENST00000639754.1:n.935G>A
ENST00000639952.1:c.732G>A	ENSP00000492697.1:p.Arg244=
ENST00000640044.1:c.310+84413G>A	ENSP00000491434.1:n.310+84413G>A
ENST00000640243.1:c.732G>A	ENSP00000492803.1:p.Arg244=
ENST00000640522.1:c.732G>A	ENSP00000491019.1:p.Arg244=
ENST00000640528.1:c.732G>A	ENSP00000491725.1:p.Arg244=
ENST00000640566.1:c.310+84413G>A	ENSP00000491302.1:n.310+84413G>A
ENST00000640710.1:c.732G>A	ENSP00000492513.1:p.Arg244=
ENST00000640890.1:n.834G>A
ENST00000271751.8:c.732G>A	ENSP00000271751.4:p.Arg244=
ENST00000367007.4:c.732G>A	ENSP00000355974.4:p.Arg244=
NM_002238.3:c.732G>A	NP_002229.1:p.Arg244=
NM_172362.2:c.732G>A	NP_758872.1:p.Arg244=
NM_172362.3:c.732G>A MANE Select	NP_758872.1:p.Arg244=
NM_002238.4:c.732G>A	NP_002229.1:p.Arg244=