Canonical Allele Identifier: CA2673782179
Gene: HCN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645122_45645123insAGCAA , CM000667.2:g.45645122_45645123insAGCAA GRCh38
NC_000005.9:g.45645224_45645225insAGCAA , CM000667.1:g.45645224_45645225insAGCAA GRCh37
NC_000005.8:g.45680981_45680982insAGCAA NCBI36
NG_042183.1:g.55996_55997insTTGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.849+62_849+63insTTGCT MANE Select ENSP00000307342.4:n.849+62_849+63insTTGCT
ENST00000637256.1:n.77+62_77+63insTTGCT
ENST00000673735.1:c.849+62_849+63insTTGCT ENSP00000501107.1:n.849+62_849+63insTTGCT
ENST00000303230.5:c.849+62_849+63insTTGCT ENSP00000307342.4:n.849+62_849+63insTTGCT
ENST00000634658.1:c.*23_*24insTTGCT ENSP00000489134.1:n.*23_*24insTTGCT
NM_021072.3:c.849+62_849+63insTTGCT NP_066550.2:n.849+62_849+63insTTGCT
NM_021072.4:c.849+62_849+63insTTGCT MANE Select NP_066550.2:n.849+62_849+63insTTGCT