Canonical Allele Identifier: CA1543688181

Gene: HCN1

Linked Data

• dbSNP Id: rs1741167277

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.45461828_45461829insGTCAGAGTGTAAAAAA , CM000667.2:g.45461828_45461829insGTCAGAGTGTAAAAAA	GRCh38
NC_000005.9:g.45461930_45461931insGTCAGAGTGTAAAAAA , CM000667.1:g.45461930_45461931insGTCAGAGTGTAAAAAA	GRCh37
NC_000005.8:g.45497687_45497688insGTCAGAGTGTAAAAAA	NCBI36
NG_042183.1:g.239294_239295insTTACACTCTGACTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303230.6:c.1011+21_1011+22insTTACACTCTGACTTTT MANE Select	ENSP00000307342.4:n.1011+21_1011+22insTTACACTCTGACTTTT
ENST00000637305.1:n.174+21_174+22insTTACACTCTGACTTTT
ENST00000673735.1:c.1011+21_1011+22insTTACACTCTGACTTTT	ENSP00000501107.1:n.1011+21_1011+22insTTACACTCTGACTTTT
ENST00000303230.5:c.1011+21_1011+22insTTACACTCTGACTTTT	ENSP00000307342.4:n.1011+21_1011+22insTTACACTCTGACTTTT
NM_021072.3:c.1011+21_1011+22insTTACACTCTGACTTTT	NP_066550.2:n.1011+21_1011+22insTTACACTCTGACTTTT
NM_021072.4:c.1011+21_1011+22insTTACACTCTGACTTTT MANE Select	NP_066550.2:n.1011+21_1011+22insTTACACTCTGACTTTT