Canonical Allele Identifier: CA344874152

Gene: KCNH1

Linked Data

• MyVariant Identifiers: chr1:g.211093366G>C (hg19) ; chr1:g.210920024G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.210920024G>C , CM000663.2:g.210920024G>C	GRCh38
NC_000001.10:g.211093366G>C , CM000663.1:g.211093366G>C	GRCh37
NC_000001.9:g.209159989G>C	NCBI36
NG_029777.1:g.219092C>G
NG_029777.2:g.219092C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271751.10:c.1078C>G MANE Select	ENSP00000271751.4:p.Arg360Gly
ENST00000367007.5:c.997C>G	ENSP00000355974.5:p.Arg333Gly
ENST00000638357.1:c.411C>G
ENST00000638498.1:c.1078C>G	ENSP00000490983.1:p.Arg360Gly
ENST00000638960.1:c.997C>G	ENSP00000492302.1:p.Arg333Gly
ENST00000638983.1:c.952-58830C>G	ENSP00000492641.1:n.952-58830C>G
ENST00000639385.1:n.446C>G
ENST00000639602.1:c.868C>G	ENSP00000492303.1:p.Arg290Gly
ENST00000639754.1:n.1281C>G
ENST00000639952.1:c.997C>G	ENSP00000492697.1:p.Arg333Gly
ENST00000640044.1:c.311-115858C>G	ENSP00000491434.1:n.311-115858C>G
ENST00000640243.1:c.951+98840C>G	ENSP00000492803.1:n.951+98840C>G
ENST00000640522.1:c.1032+98759C>G	ENSP00000491019.1:n.1032+98759C>G
ENST00000640528.1:c.997C>G	ENSP00000491725.1:p.Arg333Gly
ENST00000640566.1:c.311-144480C>G	ENSP00000491302.1:n.311-144480C>G
ENST00000640710.1:c.997C>G	ENSP00000492513.1:p.Arg333Gly
ENST00000640890.1:n.1099C>G
ENST00000271751.8:c.1078C>G	ENSP00000271751.4:p.Arg360Gly
ENST00000367007.4:c.997C>G	ENSP00000355974.4:p.Arg333Gly
NM_002238.3:c.997C>G	NP_002229.1:p.Arg333Gly
NM_172362.2:c.1078C>G	NP_758872.1:p.Arg360Gly
XM_011509514.1:c.-99C>G	XP_011507816.1:n.-99C>G
XM_017001246.1:c.-99C>G	XP_016856735.1:n.-99C>G
NM_172362.3:c.1078C>G MANE Select	NP_758872.1:p.Arg360Gly
NM_002238.4:c.997C>G	NP_002229.1:p.Arg333Gly