Canonical Allele Identifier: CA559415963

Gene: HCN1

Linked Data

• dbSNP Id: rs1561164045
• gnomAD v2: 5-45461936-G-GAGTGTAAAAAAAAAAAA
• gnomAD v3: 5-45461834-G-GAGTGTAAAAAAAAAAAA
• gnomAD v4: 5-45461834-G-GAGTGTAAAAAAAAAAAA
• MyVariant Identifiers: chr5:g.45461936_45461937insAGTGTAAAAAAAAAAAA (hg19) ; chr5:g.45461834_45461835insAGTGTAAAAAAAAAAAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.45461835_45461836insGTGTAAAAAAAAAAAAA , CM000667.2:g.45461835_45461836insGTGTAAAAAAAAAAAAA	GRCh38
NC_000005.9:g.45461937_45461938insGTGTAAAAAAAAAAAAA , CM000667.1:g.45461937_45461938insGTGTAAAAAAAAAAAAA	GRCh37
NC_000005.8:g.45497694_45497695insGTGTAAAAAAAAAAAAA	NCBI36
NG_042183.1:g.239284_239285insTTTTTTTTTTTTACACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303230.6:c.1011+11_1011+12insTTTTTTTTTTTTACACT MANE Select	ENSP00000307342.4:n.1011+11_1011+12insTTTTTTTTTTTTACACT
ENST00000637305.1:n.174+11_174+12insTTTTTTTTTTTTACACT
ENST00000673735.1:c.1011+11_1011+12insTTTTTTTTTTTTACACT	ENSP00000501107.1:n.1011+11_1011+12insTTTTTTTTTTTTACACT
ENST00000303230.5:c.1011+11_1011+12insTTTTTTTTTTTTACACT	ENSP00000307342.4:n.1011+11_1011+12insTTTTTTTTTTTTACACT
NM_021072.3:c.1011+11_1011+12insTTTTTTTTTTTTACACT	NP_066550.2:n.1011+11_1011+12insTTTTTTTTTTTTACACT
NM_021072.4:c.1011+11_1011+12insTTTTTTTTTTTTACACT MANE Select	NP_066550.2:n.1011+11_1011+12insTTTTTTTTTTTTACACT