Canonical Allele Identifier: CA2766120950

Gene: HCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.45462026_45462027insCCAAACACACCCAACAC , CM000667.2:g.45462026_45462027insCCAAACACACCCAACAC	GRCh38
NC_000005.9:g.45462128_45462129insCCAAACACACCCAACAC , CM000667.1:g.45462128_45462129insCCAAACACACCCAACAC	GRCh37
NC_000005.8:g.45497885_45497886insCCAAACACACCCAACAC	NCBI36
NG_042183.1:g.239092_239093insGTGTTGGGTGTGTTTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303230.6:c.850-20_850-19insGTGTTGGGTGTGTTTGG MANE Select	ENSP00000307342.4:n.850-20_850-19insGTGTTGGGTGTGTTTGG
ENST00000637305.1:n.13-20_13-19insGTGTTGGGTGTGTTTGG
ENST00000673735.1:c.850-20_850-19insGTGTTGGGTGTGTTTGG	ENSP00000501107.1:n.850-20_850-19insGTGTTGGGTGTGTTTGG
ENST00000303230.5:c.850-20_850-19insGTGTTGGGTGTGTTTGG	ENSP00000307342.4:n.850-20_850-19insGTGTTGGGTGTGTTTGG
NM_021072.3:c.850-20_850-19insGTGTTGGGTGTGTTTGG	NP_066550.2:n.850-20_850-19insGTGTTGGGTGTGTTTGG
NM_021072.4:c.850-20_850-19insGTGTTGGGTGTGTTTGG MANE Select	NP_066550.2:n.850-20_850-19insGTGTTGGGTGTGTTTGG