Canonical Allele Identifier: CA1543790787
Gene: HCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645577T= , CM000667.2:g.45645577T= GRCh38
NC_000005.9:g.45645679T= , CM000667.1:g.45645679T= GRCh37
NC_000005.8:g.45681436T= NCBI36
NG_042183.1:g.55542A=

Transcript Alleles

HGVS Amino-acid change
ENST00000303230.6:c.457A= MANE Select ENSP00000307342.4:p.Met153=
ENST00000673735.1:c.457A= ENSP00000501107.1:p.Met153=
ENST00000303230.5:c.457A= ENSP00000307342.4:p.Met153=
ENST00000634658.1:c.457A= ENSP00000489134.1:p.Met153=
NM_021072.3:c.457A= NP_066550.2:p.Met153=
NM_021072.4:c.457A= MANE Select NP_066550.2:p.Met153=