Canonical Allele Identifier: CA811095554
Gene: HCN1 HGNC NCBI

Linked Data

dbSNP Id: rs1461406713
MyVariant Identifiers: chr5:g.45462330_45462331del (hg19) chr5:g.45462228_45462229del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45462231_45462232del , CM000667.2:g.45462231_45462232del GRCh38
NC_000005.9:g.45462333_45462334del , CM000667.1:g.45462333_45462334del GRCh37
NC_000005.8:g.45498090_45498091del NCBI36
NG_042183.1:g.238890_238891del

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.850-222_850-221del MANE Select ENSP00000307342.4:n.850-222_850-221del
ENST00000637305.1:n.13-222_13-221del
ENST00000673735.1:c.850-222_850-221del ENSP00000501107.1:n.850-222_850-221del
ENST00000303230.5:c.850-222_850-221del ENSP00000307342.4:n.850-222_850-221del
NM_021072.3:c.850-222_850-221del NP_066550.2:n.850-222_850-221del
NM_021072.4:c.850-222_850-221del MANE Select NP_066550.2:n.850-222_850-221del
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