Canonical Allele Identifier: CA1543790148

Gene: HCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.45645134_45645135delinsTA , CM000667.2:g.45645134_45645135delinsTA	GRCh38
NC_000005.9:g.45645236_45645237delinsTA , CM000667.1:g.45645236_45645237delinsTA	GRCh37
NC_000005.8:g.45680993_45680994delinsTA	NCBI36
NG_042183.1:g.55984_55985delinsTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000303230.6:c.849+50_849+51delinsTA MANE Select	ENSP00000307342.4:n.849+50_849+51delinsTA
ENST00000637256.1:n.77+50_77+51delinsTA
ENST00000673735.1:c.849+50_849+51delinsTA	ENSP00000501107.1:n.849+50_849+51delinsTA
ENST00000303230.5:c.849+50_849+51delinsTA	ENSP00000307342.4:n.849+50_849+51delinsTA
ENST00000634658.1:c.*11_*12delinsTA	ENSP00000489134.1:n.*11_*12delinsTA
NM_021072.3:c.849+50_849+51delinsTA	NP_066550.2:n.849+50_849+51delinsTA
NM_021072.4:c.849+50_849+51delinsTA MANE Select	NP_066550.2:n.849+50_849+51delinsTA