Canonical Allele Identifier: CA2346946113
Gene: ADRA1D HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4234752_4234757delinsATACAG , CM000682.2:g.4234752_4234757delinsATACAG GRCh38
NC_000020.10:g.4215399_4215404delinsATACAG , CM000682.1:g.4215399_4215404delinsATACAG GRCh37
NC_000020.9:g.4163399_4163404delinsATACAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000379453.6:c.1112-12627_1112-12622delinsCTGTAT MANE Select ENSP00000368766.4:n.1112-12627_1112-12622delinsCTGTAT
ENST00000379453.5:c.1112-12627_1112-12622delinsCTGTAT ENSP00000368766.4:n.1112-12627_1112-12622delinsCTGTAT
NM_000678.3:c.1112-12627_1112-12622delinsCTGTAT NP_000669.1:n.1112-12627_1112-12622delinsCTGTAT
NM_000678.4:c.1112-12627_1112-12622delinsCTGTAT MANE Select NP_000669.1:n.1112-12627_1112-12622delinsCTGTAT
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