Canonical Allele Identifier: CA1543790873

Gene: HCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.45645660_45645661delinsTC , CM000667.2:g.45645660_45645661delinsTC	GRCh38
NC_000005.9:g.45645762_45645763delinsTC , CM000667.1:g.45645762_45645763delinsTC	GRCh37
NC_000005.8:g.45681519_45681520delinsTC	NCBI36
NG_042183.1:g.55458_55459delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303230.6:c.426-53_426-52delinsGA MANE Select	ENSP00000307342.4:n.426-53_426-52delinsGA
ENST00000673735.1:c.426-53_426-52delinsGA	ENSP00000501107.1:n.426-53_426-52delinsGA
ENST00000303230.5:c.426-53_426-52delinsGA	ENSP00000307342.4:n.426-53_426-52delinsGA
ENST00000634658.1:c.426-53_426-52delinsGA	ENSP00000489134.1:n.426-53_426-52delinsGA
NM_021072.3:c.426-53_426-52delinsGA	NP_066550.2:n.426-53_426-52delinsGA
NM_021072.4:c.426-53_426-52delinsGA MANE Select	NP_066550.2:n.426-53_426-52delinsGA