Canonical Allele Identifier: CA2527478261

Gene: HCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.45462021_45462028del , CM000667.2:g.45462021_45462028del	GRCh38
NC_000005.9:g.45462123_45462130del , CM000667.1:g.45462123_45462130del	GRCh37
NC_000005.8:g.45497880_45497887del	NCBI36
NG_042183.1:g.239091_239098del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303230.6:c.850-21_850-14del MANE Select	ENSP00000307342.4:n.850-21_850-14del
ENST00000637305.1:n.13-21_13-14del
ENST00000673735.1:c.850-21_850-14del	ENSP00000501107.1:n.850-21_850-14del
ENST00000303230.5:c.850-21_850-14del	ENSP00000307342.4:n.850-21_850-14del
NM_021072.3:c.850-21_850-14del	NP_066550.2:n.850-21_850-14del
NM_021072.4:c.850-21_850-14del MANE Select	NP_066550.2:n.850-21_850-14del