Canonical Allele Identifier: CA2484788431
Gene: KCNH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.210804215_210804236delinsCCTGAGCCAGGGTTCCAGAATG , CM000663.2:g.210804215_210804236delinsCCTGAGCCAGGGTTCCAGAATG GRCh38
NC_000001.10:g.210977557_210977578delinsCCTGAGCCAGGGTTCCAGAATG , CM000663.1:g.210977557_210977578delinsCCTGAGCCAGGGTTCCAGAATG GRCh37
NC_000001.9:g.209044180_209044201delinsCCTGAGCCAGGGTTCCAGAATG NCBI36
NG_029777.1:g.334880_334901delinsCATTCTGGAACCCTGGCTCAGG
NG_029777.2:g.334880_334901delinsCATTCTGGAACCCTGGCTCAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000271751.10:c.1463-70_1463-49delinsCATTCTGGAACCCTGGCTCAGG MANE Select ENSP00000271751.4:n.1463-70_1463-49delinsCATTCTGGAACCCTGGCTCA...
ENST00000367007.5:c.1382-70_1382-49delinsCATTCTGGAACCCTGGCTCAGG ENSP00000355974.5:n.1382-70_1382-49delinsCATTCTGGAACCCTGGCTCA...
ENST00000638357.1:c.796-70_796-49delinsCATTCTGGAACCCTGGCTCAGG
ENST00000638498.1:c.1463-70_1463-49delinsCATTCTGGAACCCTGGCTCAGG ENSP00000490983.1:n.1463-70_1463-49delinsCATTCTGGAACCCTGGCTCA...
ENST00000638960.1:c.1382-70_1382-49delinsCATTCTGGAACCCTGGCTCAGG ENSP00000492302.1:n.1382-70_1382-49delinsCATTCTGGAACCCTGGCTCA...
ENST00000639952.1:c.1382-70_1382-49delinsCATTCTGGAACCCTGGCTCAGG ENSP00000492697.1:n.1382-70_1382-49delinsCATTCTGGAACCCTGGCTCA...
ENST00000640044.1:c.311-70_311-49delinsCATTCTGGAACCCTGGCTCAGG ENSP00000491434.1:n.311-70_311-49delinsCATTCTGGAACCCTGGCTCAGG...
ENST00000640243.1:c.952-70_952-49delinsCATTCTGGAACCCTGGCTCAGG ENSP00000492803.1:n.952-70_952-49delinsCATTCTGGAACCCTGGCTCAGG...
ENST00000640522.1:c.1033-70_1033-49delinsCATTCTGGAACCCTGGCTCAGG ENSP00000491019.1:n.1033-70_1033-49delinsCATTCTGGAACCCTGGCTCA...
ENST00000640528.1:c.1382-70_1382-49delinsCATTCTGGAACCCTGGCTCAGG ENSP00000491725.1:n.1382-70_1382-49delinsCATTCTGGAACCCTGGCTCA...
ENST00000640566.1:c.311-28692_311-28671delinsCATTCTGGAACCCTGGCTCAGG ENSP00000491302.1:n.311-28692_311-28671delinsCATTCTGGAACCCTGG...
ENST00000640710.1:c.1382-70_1382-49delinsCATTCTGGAACCCTGGCTCAGG ENSP00000492513.1:n.1382-70_1382-49delinsCATTCTGGAACCCTGGCTCA...
ENST00000271751.8:c.1463-70_1463-49delinsCATTCTGGAACCCTGGCTCAGG ENSP00000271751.4:n.1463-70_1463-49delinsCATTCTGGAACCCTGGCTCA...
ENST00000367007.4:c.1382-70_1382-49delinsCATTCTGGAACCCTGGCTCAGG ENSP00000355974.4:n.1382-70_1382-49delinsCATTCTGGAACCCTGGCTCA...
NM_002238.3:c.1382-70_1382-49delinsCATTCTGGAACCCTGGCTCAGG NP_002229.1:n.1382-70_1382-49delinsCATTCTGGAACCCTGGCTCAGG
NM_172362.2:c.1463-70_1463-49delinsCATTCTGGAACCCTGGCTCAGG NP_758872.1:n.1463-70_1463-49delinsCATTCTGGAACCCTGGCTCAGG
XM_011509514.1:c.287-70_287-49delinsCATTCTGGAACCCTGGCTCAGG XP_011507816.1:n.287-70_287-49delinsCATTCTGGAACCCTGGCTCAGG
XM_017001246.1:c.287-70_287-49delinsCATTCTGGAACCCTGGCTCAGG XP_016856735.1:n.287-70_287-49delinsCATTCTGGAACCCTGGCTCAGG
NM_172362.3:c.1463-70_1463-49delinsCATTCTGGAACCCTGGCTCAGG MANE Select NP_758872.1:n.1463-70_1463-49delinsCATTCTGGAACCCTGGCTCAGG
NM_002238.4:c.1382-70_1382-49delinsCATTCTGGAACCCTGGCTCAGG NP_002229.1:n.1382-70_1382-49delinsCATTCTGGAACCCTGGCTCAGG