Canonical Allele Identifier: CA1543790452
Gene: HCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645323A= , CM000667.2:g.45645323A= GRCh38
NC_000005.9:g.45645425A= , CM000667.1:g.45645425A= GRCh37
NC_000005.8:g.45681182A= NCBI36
NG_042183.1:g.55796T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.711T= MANE Select ENSP00000307342.4:p.Leu237=
ENST00000673735.1:c.711T= ENSP00000501107.1:p.Leu237=
ENST00000303230.5:c.711T= ENSP00000307342.4:p.Leu237=
ENST00000634658.1:c.711T= ENSP00000489134.1:p.Leu237=
NM_021072.3:c.711T= NP_066550.2:p.Leu237=
NM_021072.4:c.711T= MANE Select NP_066550.2:p.Leu237=