Canonical Allele Identifier: CA37156768

Gene: KCNH1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.211083095C>T , CM000663.2:g.211083095C>T	GRCh38
NC_000001.10:g.211256437C>T , CM000663.1:g.211256437C>T	GRCh37
NC_000001.9:g.209323060C>T	NCBI36
NG_029777.1:g.56021G>A
NG_029777.2:g.56021G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_172362.3:c.440-197G>A MANE Select	NP_758872.1:n.440-197G>A
ENST00000271751.10:c.440-197G>A MANE Select	ENSP00000271751.4:n.440-197G>A
NM_002238.3:c.440-197G>A	NP_002229.1:n.440-197G>A
NM_002238.4:c.440-197G>A	NP_002229.1:n.440-197G>A
NM_172362.2:c.440-197G>A	NP_758872.1:n.440-197G>A
ENST00000271751.8:c.440-197G>A	ENSP00000271751.4:n.440-197G>A
ENST00000367007.4:c.440-197G>A	ENSP00000355974.4:n.440-197G>A
ENST00000367007.5:c.440-197G>A	ENSP00000355974.5:n.440-197G>A
ENST00000624583.2:n.150-197G>A
ENST00000638498.1:c.440-197G>A	ENSP00000490983.1:n.440-197G>A
ENST00000638880.1:c.260-197G>A	ENSP00000491750.1:n.260-197G>A
ENST00000638960.1:c.440-197G>A	ENSP00000492302.1:n.440-197G>A
ENST00000638983.1:c.440-197G>A	ENSP00000492641.1:n.440-197G>A
ENST00000639602.1:c.311-197G>A	ENSP00000492303.1:n.311-197G>A
ENST00000639754.1:n.643-197G>A
ENST00000639952.1:c.440-197G>A	ENSP00000492697.1:n.440-197G>A
ENST00000640044.1:c.310+20401G>A	ENSP00000491434.1:n.310+20401G>A
ENST00000640243.1:c.440-197G>A	ENSP00000492803.1:n.440-197G>A
ENST00000640522.1:c.440-197G>A	ENSP00000491019.1:n.440-197G>A
ENST00000640528.1:c.440-197G>A	ENSP00000491725.1:n.440-197G>A
ENST00000640566.1:c.310+20401G>A	ENSP00000491302.1:n.310+20401G>A
ENST00000640710.1:c.440-197G>A	ENSP00000492513.1:n.440-197G>A
ENST00000640890.1:n.542-197G>A