Canonical Allele Identifier: CA1820608999
Gene: HHLA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132090943_132090949delinsTAGAGAC , CM000670.2:g.132090943_132090949delinsTAGAGAC GRCh38
NC_000008.10:g.133103190_133103196delinsTAGAGAC , CM000670.1:g.133103190_133103196delinsTAGAGAC GRCh37
NC_000008.9:g.133172372_133172378delinsTAGAGAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000414222.2:c.449-1350_449-1344delinsGTCTCTA MANE Select ENSP00000388322.1:n.449-1350_449-1344delinsGTCTCTA
ENST00000673615.1:c.557-1350_557-1344delinsGTCTCTA ENSP00000500443.1:n.557-1350_557-1344delinsGTCTCTA
ENST00000414222.1:c.449-1350_449-1344delinsGTCTCTA ENSP00000388322.1:n.449-1350_449-1344delinsGTCTCTA
ENST00000434736.6:c.557-1350_557-1344delinsGTCTCTA ENSP00000407107.2:n.557-1350_557-1344delinsGTCTCTA
NM_001145095.1:c.449-1350_449-1344delinsGTCTCTA NP_001138567.1:n.449-1350_449-1344delinsGTCTCTA
NM_001145095.3:c.449-1350_449-1344delinsGTCTCTA MANE Select NP_001138567.1:n.449-1350_449-1344delinsGTCTCTA