Canonical Allele Identifier: CA423145947

Gene: KCNH1

Linked Data

• MyVariant Identifiers: chr1:g.211093214G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.210919872G>A , CM000663.2:g.210919872G>A	GRCh38
NC_000001.10:g.211093214G>A , CM000663.1:g.211093214G>A	GRCh37
NC_000001.9:g.209159837G>A	NCBI36
NG_029777.1:g.219244C>T
NG_029777.2:g.219244C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000271751.10:c.1230C>T MANE Select	ENSP00000271751.4:p.Thr410=
ENST00000367007.5:c.1149C>T	ENSP00000355974.5:p.Thr383=
ENST00000638357.1:c.563C>T
ENST00000638498.1:c.1230C>T	ENSP00000490983.1:p.Thr410=
ENST00000638960.1:c.1149C>T	ENSP00000492302.1:p.Thr383=
ENST00000638983.1:c.952-58678C>T	ENSP00000492641.1:n.952-58678C>T
ENST00000639385.1:n.598C>T
ENST00000639602.1:c.1020C>T	ENSP00000492303.1:p.Thr340=
ENST00000639754.1:n.1433C>T
ENST00000639952.1:c.1149C>T	ENSP00000492697.1:p.Thr383=
ENST00000640044.1:c.311-115706C>T	ENSP00000491434.1:n.311-115706C>T
ENST00000640243.1:c.951+98992C>T	ENSP00000492803.1:n.951+98992C>T
ENST00000640522.1:c.1032+98911C>T	ENSP00000491019.1:n.1032+98911C>T
ENST00000640528.1:c.1149C>T	ENSP00000491725.1:p.Thr383=
ENST00000640566.1:c.311-144328C>T	ENSP00000491302.1:n.311-144328C>T
ENST00000640710.1:c.1149C>T	ENSP00000492513.1:p.Thr383=
ENST00000640890.1:n.1251C>T
ENST00000271751.8:c.1230C>T	ENSP00000271751.4:p.Thr410=
ENST00000367007.4:c.1149C>T	ENSP00000355974.4:p.Thr383=
NM_002238.3:c.1149C>T	NP_002229.1:p.Thr383=
NM_172362.2:c.1230C>T	NP_758872.1:p.Thr410=
XM_011509514.1:c.54C>T	XP_011507816.1:p.Thr18=
XM_017001246.1:c.54C>T	XP_016856735.1:p.Thr18=
NM_172362.3:c.1230C>T MANE Select	NP_758872.1:p.Thr410=
NM_002238.4:c.1149C>T	NP_002229.1:p.Thr383=