Canonical Allele Identifier: CA2573131641

Gene: KCNH1

Linked Data

• ClinVar Variation Id: 1546388
• ClinVar RCV Id: RCV002170751
• dbSNP Id: rs2102561909

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.210920079G>A , CM000663.2:g.210920079G>A	GRCh38
NC_000001.10:g.211093421G>A , CM000663.1:g.211093421G>A	GRCh37
NC_000001.9:g.209160044G>A	NCBI36
NG_029777.1:g.219037C>T
NG_029777.2:g.219037C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271751.10:c.1033-10C>T MANE Select	ENSP00000271751.4:n.1033-10C>T
ENST00000367007.5:c.952-10C>T	ENSP00000355974.5:n.952-10C>T
ENST00000638357.1:c.366-10C>T
ENST00000638498.1:c.1033-10C>T	ENSP00000490983.1:n.1033-10C>T
ENST00000638960.1:c.952-10C>T	ENSP00000492302.1:n.952-10C>T
ENST00000638983.1:c.952-58885C>T	ENSP00000492641.1:n.952-58885C>T
ENST00000639385.1:n.409-18C>T
ENST00000639602.1:c.823-10C>T	ENSP00000492303.1:n.823-10C>T
ENST00000639754.1:n.1236-10C>T
ENST00000639952.1:c.952-10C>T	ENSP00000492697.1:n.952-10C>T
ENST00000640044.1:c.311-115913C>T	ENSP00000491434.1:n.311-115913C>T
ENST00000640243.1:c.951+98785C>T	ENSP00000492803.1:n.951+98785C>T
ENST00000640522.1:c.1032+98704C>T	ENSP00000491019.1:n.1032+98704C>T
ENST00000640528.1:c.952-10C>T	ENSP00000491725.1:n.952-10C>T
ENST00000640566.1:c.311-144535C>T	ENSP00000491302.1:n.311-144535C>T
ENST00000640710.1:c.952-10C>T	ENSP00000492513.1:n.952-10C>T
ENST00000640890.1:n.1054-10C>T
ENST00000271751.8:c.1033-10C>T	ENSP00000271751.4:n.1033-10C>T
ENST00000367007.4:c.952-10C>T	ENSP00000355974.4:n.952-10C>T
NM_002238.3:c.952-10C>T	NP_002229.1:n.952-10C>T
NM_172362.2:c.1033-10C>T	NP_758872.1:n.1033-10C>T
XM_011509514.1:c.-144-10C>T	XP_011507816.1:n.-144-10C>T
XM_017001246.1:c.-144-10C>T	XP_016856735.1:n.-144-10C>T
NM_172362.3:c.1033-10C>T MANE Select	NP_758872.1:n.1033-10C>T
NM_002238.4:c.952-10C>T	NP_002229.1:n.952-10C>T