Canonical Allele Identifier: CA2650361904
Gene: KCNH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.210804299_210804307del , CM000663.2:g.210804299_210804307del GRCh38
NC_000001.10:g.210977641_210977649del , CM000663.1:g.210977641_210977649del GRCh37
NC_000001.9:g.209044264_209044272del NCBI36
NG_029777.1:g.334810_334818del
NG_029777.2:g.334810_334818del

Transcript Alleles

HGVS Amino-acid Change
ENST00000271751.10:c.1463-140_1463-132del MANE Select ENSP00000271751.4:n.1463-140_1463-132del
ENST00000367007.5:c.1382-140_1382-132del ENSP00000355974.5:n.1382-140_1382-132del
ENST00000638357.1:c.796-140_796-132del
ENST00000638498.1:c.1463-140_1463-132del ENSP00000490983.1:n.1463-140_1463-132del
ENST00000638960.1:c.1382-140_1382-132del ENSP00000492302.1:n.1382-140_1382-132del
ENST00000639952.1:c.1382-140_1382-132del ENSP00000492697.1:n.1382-140_1382-132del
ENST00000640044.1:c.311-140_311-132del ENSP00000491434.1:n.311-140_311-132del
ENST00000640243.1:c.952-140_952-132del ENSP00000492803.1:n.952-140_952-132del
ENST00000640522.1:c.1033-140_1033-132del ENSP00000491019.1:n.1033-140_1033-132del
ENST00000640528.1:c.1382-140_1382-132del ENSP00000491725.1:n.1382-140_1382-132del
ENST00000640566.1:c.311-28762_311-28754del ENSP00000491302.1:n.311-28762_311-28754del
ENST00000640710.1:c.1382-140_1382-132del ENSP00000492513.1:n.1382-140_1382-132del
ENST00000271751.8:c.1463-140_1463-132del ENSP00000271751.4:n.1463-140_1463-132del
ENST00000367007.4:c.1382-140_1382-132del ENSP00000355974.4:n.1382-140_1382-132del
NM_002238.3:c.1382-140_1382-132del NP_002229.1:n.1382-140_1382-132del
NM_172362.2:c.1463-140_1463-132del NP_758872.1:n.1463-140_1463-132del
XM_011509514.1:c.287-140_287-132del XP_011507816.1:n.287-140_287-132del
XM_017001246.1:c.287-140_287-132del XP_016856735.1:n.287-140_287-132del
NM_172362.3:c.1463-140_1463-132del MANE Select NP_758872.1:n.1463-140_1463-132del
NM_002238.4:c.1382-140_1382-132del NP_002229.1:n.1382-140_1382-132del