Canonical Allele Identifier: CA344873585

Gene: KCNH1

Linked Data

• MyVariant Identifiers: chr1:g.211093235A>T (hg19) ; chr1:g.210919893A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.210919893A>T , CM000663.2:g.210919893A>T	GRCh38
NC_000001.10:g.211093235A>T , CM000663.1:g.211093235A>T	GRCh37
NC_000001.9:g.209159858A>T	NCBI36
NG_029777.1:g.219223T>A
NG_029777.2:g.219223T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000271751.10:c.1209T>A MANE Select	ENSP00000271751.4:p.Tyr403Ter
ENST00000367007.5:c.1128T>A	ENSP00000355974.5:p.Tyr376Ter
ENST00000638357.1:c.542T>A
ENST00000638498.1:c.1209T>A	ENSP00000490983.1:p.Tyr403Ter
ENST00000638960.1:c.1128T>A	ENSP00000492302.1:p.Tyr376Ter
ENST00000638983.1:c.952-58699T>A	ENSP00000492641.1:n.952-58699T>A
ENST00000639385.1:n.577T>A
ENST00000639602.1:c.999T>A	ENSP00000492303.1:p.Tyr333Ter
ENST00000639754.1:n.1412T>A
ENST00000639952.1:c.1128T>A	ENSP00000492697.1:p.Tyr376Ter
ENST00000640044.1:c.311-115727T>A	ENSP00000491434.1:n.311-115727T>A
ENST00000640243.1:c.951+98971T>A	ENSP00000492803.1:n.951+98971T>A
ENST00000640522.1:c.1032+98890T>A	ENSP00000491019.1:n.1032+98890T>A
ENST00000640528.1:c.1128T>A	ENSP00000491725.1:p.Tyr376Ter
ENST00000640566.1:c.311-144349T>A	ENSP00000491302.1:n.311-144349T>A
ENST00000640710.1:c.1128T>A	ENSP00000492513.1:p.Tyr376Ter
ENST00000640890.1:n.1230T>A
ENST00000271751.8:c.1209T>A	ENSP00000271751.4:p.Tyr403Ter
ENST00000367007.4:c.1128T>A	ENSP00000355974.4:p.Tyr376Ter
NM_002238.3:c.1128T>A	NP_002229.1:p.Tyr376Ter
NM_172362.2:c.1209T>A	NP_758872.1:p.Tyr403Ter
XM_011509514.1:c.33T>A	XP_011507816.1:p.Tyr11Ter
XM_017001246.1:c.33T>A	XP_016856735.1:p.Tyr11Ter
NM_172362.3:c.1209T>A MANE Select	NP_758872.1:p.Tyr403Ter
NM_002238.4:c.1128T>A	NP_002229.1:p.Tyr376Ter