Canonical Allele Identifier: CA1543688768
Gene: HCN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45462283_45462284delinsGT , CM000667.2:g.45462283_45462284delinsGT GRCh38
NC_000005.9:g.45462385_45462386delinsGT , CM000667.1:g.45462385_45462386delinsGT GRCh37
NC_000005.8:g.45498142_45498143delinsGT NCBI36
NG_042183.1:g.238835_238836delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.850-277_850-276delinsAC MANE Select ENSP00000307342.4:n.850-277_850-276delinsAC
ENST00000637305.1:n.13-277_13-276delinsAC
ENST00000673735.1:c.850-277_850-276delinsAC ENSP00000501107.1:n.850-277_850-276delinsAC
ENST00000303230.5:c.850-277_850-276delinsAC ENSP00000307342.4:n.850-277_850-276delinsAC
NM_021072.3:c.850-277_850-276delinsAC NP_066550.2:n.850-277_850-276delinsAC
NM_021072.4:c.850-277_850-276delinsAC MANE Select NP_066550.2:n.850-277_850-276delinsAC
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