Canonical Allele Identifier: CA1543790154
Gene: HCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645134T= , CM000667.2:g.45645134T= GRCh38
NC_000005.9:g.45645236T= , CM000667.1:g.45645236T= GRCh37
NC_000005.8:g.45680993T= NCBI36
NG_042183.1:g.55985A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.849+51A= MANE Select ENSP00000307342.4:n.849+51A=
ENST00000637256.1:n.77+51A=
ENST00000673735.1:c.849+51A= ENSP00000501107.1:n.849+51A=
ENST00000303230.5:c.849+51A= ENSP00000307342.4:n.849+51A=
ENST00000634658.1:c.*12A= ENSP00000489134.1:n.*12A=
NM_021072.3:c.849+51A= NP_066550.2:n.849+51A=
NM_021072.4:c.849+51A= MANE Select NP_066550.2:n.849+51A=