Canonical Allele Identifier: CA2673782253
Gene: HCN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45645682_45645683del , CM000667.2:g.45645682_45645683del GRCh38
NC_000005.9:g.45645784_45645785del , CM000667.1:g.45645784_45645785del GRCh37
NC_000005.8:g.45681541_45681542del NCBI36
NG_042183.1:g.55436_55437del

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.426-75_426-74del MANE Select ENSP00000307342.4:n.426-75_426-74del
ENST00000673735.1:c.426-75_426-74del ENSP00000501107.1:n.426-75_426-74del
ENST00000303230.5:c.426-75_426-74del ENSP00000307342.4:n.426-75_426-74del
ENST00000634658.1:c.426-75_426-74del ENSP00000489134.1:n.426-75_426-74del
NM_021072.3:c.426-75_426-74del NP_066550.2:n.426-75_426-74del
NM_021072.4:c.426-75_426-74del MANE Select NP_066550.2:n.426-75_426-74del