Canonical Allele Identifier: CA1543790798
Gene: HCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645583T= , CM000667.2:g.45645583T= GRCh38
NC_000005.9:g.45645685T= , CM000667.1:g.45645685T= GRCh37
NC_000005.8:g.45681442T= NCBI36
NG_042183.1:g.55536A=

Transcript Alleles

HGVS Amino-acid change
ENST00000303230.6:c.451A= MANE Select ENSP00000307342.4:p.Ile151=
ENST00000673735.1:c.451A= ENSP00000501107.1:p.Ile151=
ENST00000303230.5:c.451A= ENSP00000307342.4:p.Ile151=
ENST00000634658.1:c.451A= ENSP00000489134.1:p.Ile151=
NM_021072.3:c.451A= NP_066550.2:p.Ile151=
NM_021072.4:c.451A= MANE Select NP_066550.2:p.Ile151=