Canonical Allele Identifier: CA1543688260
Gene: HCN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45461877G= , CM000667.2:g.45461877G= GRCh38
NC_000005.9:g.45461979G= , CM000667.1:g.45461979G= GRCh37
NC_000005.8:g.45497736G= NCBI36
NG_042183.1:g.239242C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.980C= MANE Select ENSP00000307342.4:p.Pro327=
ENST00000637305.1:n.143C=
ENST00000673735.1:c.980C= ENSP00000501107.1:p.Pro327=
ENST00000303230.5:c.980C= ENSP00000307342.4:p.Pro327=
NM_021072.3:c.980C= NP_066550.2:p.Pro327=
NM_021072.4:c.980C= MANE Select NP_066550.2:p.Pro327=
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