Canonical Allele Identifier: CA344873773

Gene: KCNH1

Linked Data

• MyVariant Identifiers: chr1:g.211093284C>G (hg19) ; chr1:g.210919942C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.210919942C>G , CM000663.2:g.210919942C>G	GRCh38
NC_000001.10:g.211093284C>G , CM000663.1:g.211093284C>G	GRCh37
NC_000001.9:g.209159907C>G	NCBI36
NG_029777.1:g.219174G>C
NG_029777.2:g.219174G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271751.10:c.1160G>C MANE Select	ENSP00000271751.4:p.Gly387Ala
ENST00000367007.5:c.1079G>C	ENSP00000355974.5:p.Gly360Ala
ENST00000638357.1:c.493G>C
ENST00000638498.1:c.1160G>C	ENSP00000490983.1:p.Gly387Ala
ENST00000638960.1:c.1079G>C	ENSP00000492302.1:p.Gly360Ala
ENST00000638983.1:c.952-58748G>C	ENSP00000492641.1:n.952-58748G>C
ENST00000639385.1:n.528G>C
ENST00000639602.1:c.950G>C	ENSP00000492303.1:p.Gly317Ala
ENST00000639754.1:n.1363G>C
ENST00000639952.1:c.1079G>C	ENSP00000492697.1:p.Gly360Ala
ENST00000640044.1:c.311-115776G>C	ENSP00000491434.1:n.311-115776G>C
ENST00000640243.1:c.951+98922G>C	ENSP00000492803.1:n.951+98922G>C
ENST00000640522.1:c.1032+98841G>C	ENSP00000491019.1:n.1032+98841G>C
ENST00000640528.1:c.1079G>C	ENSP00000491725.1:p.Gly360Ala
ENST00000640566.1:c.311-144398G>C	ENSP00000491302.1:n.311-144398G>C
ENST00000640710.1:c.1079G>C	ENSP00000492513.1:p.Gly360Ala
ENST00000640890.1:n.1181G>C
ENST00000271751.8:c.1160G>C	ENSP00000271751.4:p.Gly387Ala
ENST00000367007.4:c.1079G>C	ENSP00000355974.4:p.Gly360Ala
NM_002238.3:c.1079G>C	NP_002229.1:p.Gly360Ala
NM_172362.2:c.1160G>C	NP_758872.1:p.Gly387Ala
XM_011509514.1:c.-17G>C	XP_011507816.1:n.-17G>C
XM_017001246.1:c.-17G>C	XP_016856735.1:n.-17G>C
NM_172362.3:c.1160G>C MANE Select	NP_758872.1:p.Gly387Ala
NM_002238.4:c.1079G>C	NP_002229.1:p.Gly360Ala