Canonical Allele Identifier: CA1543688444
Gene: HCN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45461987A= , CM000667.2:g.45461987A= GRCh38
NC_000005.9:g.45462089A= , CM000667.1:g.45462089A= GRCh37
NC_000005.8:g.45497846A= NCBI36
NG_042183.1:g.239132T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.870T= MANE Select ENSP00000307342.4:p.Asp290=
ENST00000637305.1:n.33T=
ENST00000673735.1:c.870T= ENSP00000501107.1:p.Asp290=
ENST00000303230.5:c.870T= ENSP00000307342.4:p.Asp290=
NM_021072.3:c.870T= NP_066550.2:p.Asp290=
NM_021072.4:c.870T= MANE Select NP_066550.2:p.Asp290=
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