Canonical Allele Identifier: CA118303578
Gene: HCN1 HGNC NCBI

Linked Data

dbSNP Id: rs200576945
MyVariant Identifiers: chr5:g.45462393_45462394insTTA (hg19) chr5:g.45462291_45462292insTTA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45462292_45462293insTAT , CM000667.2:g.45462292_45462293insTAT GRCh38
NC_000005.9:g.45462394_45462395insTAT , CM000667.1:g.45462394_45462395insTAT GRCh37
NC_000005.8:g.45498151_45498152insTAT NCBI36
NG_042183.1:g.238827_238828insTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000303230.6:c.850-285_850-284insTAA MANE Select ENSP00000307342.4:n.850-285_850-284insTAA
ENST00000637305.1:n.13-285_13-284insTAA
ENST00000673735.1:c.850-285_850-284insTAA ENSP00000501107.1:n.850-285_850-284insTAA
ENST00000303230.5:c.850-285_850-284insTAA ENSP00000307342.4:n.850-285_850-284insTAA
NM_021072.3:c.850-285_850-284insTAA NP_066550.2:n.850-285_850-284insTAA
NM_021072.4:c.850-285_850-284insTAA MANE Select NP_066550.2:n.850-285_850-284insTAA
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