Canonical Allele Identifier: CA2673782180

Gene: HCN1

Linked Data

• gnomAD v4: 5-45645125-A-ATT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.45645125_45645126insTT , CM000667.2:g.45645125_45645126insTT	GRCh38
NC_000005.9:g.45645227_45645228insTT , CM000667.1:g.45645227_45645228insTT	GRCh37
NC_000005.8:g.45680984_45680985insTT	NCBI36
NG_042183.1:g.55993_55994insAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000303230.6:c.849+59_849+60insAA MANE Select	ENSP00000307342.4:n.849+59_849+60insAA
ENST00000637256.1:n.77+59_77+60insAA
ENST00000673735.1:c.849+59_849+60insAA	ENSP00000501107.1:n.849+59_849+60insAA
ENST00000303230.5:c.849+59_849+60insAA	ENSP00000307342.4:n.849+59_849+60insAA
ENST00000634658.1:c.*20_*21insAA	ENSP00000489134.1:n.*20_*21insAA
NM_021072.3:c.849+59_849+60insAA	NP_066550.2:n.849+59_849+60insAA
NM_021072.4:c.849+59_849+60insAA MANE Select	NP_066550.2:n.849+59_849+60insAA