Canonical Allele Identifier: CA1543790657
Gene: HCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645485A= , CM000667.2:g.45645485A= GRCh38
NC_000005.9:g.45645587A= , CM000667.1:g.45645587A= GRCh37
NC_000005.8:g.45681344A= NCBI36
NG_042183.1:g.55634T=

Transcript Alleles

HGVS Amino-acid change
ENST00000303230.6:c.549T= MANE Select ENSP00000307342.4:p.Asp183=
ENST00000673735.1:c.549T= ENSP00000501107.1:p.Asp183=
ENST00000303230.5:c.549T= ENSP00000307342.4:p.Asp183=
ENST00000634658.1:c.549T= ENSP00000489134.1:p.Asp183=
NM_021072.3:c.549T= NP_066550.2:p.Asp183=
NM_021072.4:c.549T= MANE Select NP_066550.2:p.Asp183=