Canonical Allele Identifier: CA2673782176
Gene: HCN1 HGNC NCBI

Linked Data

gnomAD v4: 5-45645120-T-TTTA
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645121_45645122insTAT , CM000667.2:g.45645121_45645122insTAT GRCh38
NC_000005.9:g.45645223_45645224insTAT , CM000667.1:g.45645223_45645224insTAT GRCh37
NC_000005.8:g.45680980_45680981insTAT NCBI36
NG_042183.1:g.55998_55999insTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.849+64_849+65insTAA MANE Select ENSP00000307342.4:n.849+64_849+65insTAA
ENST00000637256.1:n.77+64_77+65insTAA
ENST00000673735.1:c.849+64_849+65insTAA ENSP00000501107.1:n.849+64_849+65insTAA
ENST00000303230.5:c.849+64_849+65insTAA ENSP00000307342.4:n.849+64_849+65insTAA
ENST00000634658.1:c.*25_*26insTAA ENSP00000489134.1:n.*25_*26insTAA
NM_021072.3:c.849+64_849+65insTAA NP_066550.2:n.849+64_849+65insTAA
NM_021072.4:c.849+64_849+65insTAA MANE Select NP_066550.2:n.849+64_849+65insTAA
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