Canonical Allele Identifier: CA559415949

Gene: HCN1

Linked Data

• dbSNP Id: rs1365166417
• gnomAD v2: 5-45461930-A-AG
• gnomAD v3: 5-45461828-A-AG
• gnomAD v4: 5-45461828-A-AG
• MyVariant Identifiers: chr5:g.45461930_45461931insG (hg19) ; chr5:g.45461828_45461829insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.45461828_45461829insG , CM000667.2:g.45461828_45461829insG	GRCh38
NC_000005.9:g.45461930_45461931insG , CM000667.1:g.45461930_45461931insG	GRCh37
NC_000005.8:g.45497687_45497688insG	NCBI36
NG_042183.1:g.239290_239291insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303230.6:c.1011+17_1011+18insC MANE Select	ENSP00000307342.4:n.1011+17_1011+18insC
ENST00000637305.1:n.174+17_174+18insC
ENST00000673735.1:c.1011+17_1011+18insC	ENSP00000501107.1:n.1011+17_1011+18insC
ENST00000303230.5:c.1011+17_1011+18insC	ENSP00000307342.4:n.1011+17_1011+18insC
NM_021072.3:c.1011+17_1011+18insC	NP_066550.2:n.1011+17_1011+18insC
NM_021072.4:c.1011+17_1011+18insC MANE Select	NP_066550.2:n.1011+17_1011+18insC