Canonical Allele Identifier: CA1820609139
Gene: HHLA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132091082_132091086delinsCTTAG , CM000670.2:g.132091082_132091086delinsCTTAG GRCh38
NC_000008.10:g.133103329_133103333delinsCTTAG , CM000670.1:g.133103329_133103333delinsCTTAG GRCh37
NC_000008.9:g.133172511_133172515delinsCTTAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000414222.2:c.449-1487_449-1483delinsCTAAG MANE Select ENSP00000388322.1:n.449-1487_449-1483delinsCTAAG
ENST00000673615.1:c.557-1487_557-1483delinsCTAAG ENSP00000500443.1:n.557-1487_557-1483delinsCTAAG
ENST00000414222.1:c.449-1487_449-1483delinsCTAAG ENSP00000388322.1:n.449-1487_449-1483delinsCTAAG
ENST00000434736.6:c.557-1487_557-1483delinsCTAAG ENSP00000407107.2:n.557-1487_557-1483delinsCTAAG
NM_001145095.1:c.449-1487_449-1483delinsCTAAG NP_001138567.1:n.449-1487_449-1483delinsCTAAG
NM_001145095.3:c.449-1487_449-1483delinsCTAAG MANE Select NP_001138567.1:n.449-1487_449-1483delinsCTAAG
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