Canonical Allele Identifier: CA1820609057
Gene: HHLA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132090998C= , CM000670.2:g.132090998C= GRCh38
NC_000008.10:g.133103245C= , CM000670.1:g.133103245C= GRCh37
NC_000008.9:g.133172427C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000414222.2:c.449-1399G= MANE Select ENSP00000388322.1:n.449-1399G=
ENST00000673615.1:c.557-1399G= ENSP00000500443.1:n.557-1399G=
ENST00000414222.1:c.449-1399G= ENSP00000388322.1:n.449-1399G=
ENST00000434736.6:c.557-1399G= ENSP00000407107.2:n.557-1399G=
NM_001145095.1:c.449-1399G= NP_001138567.1:n.449-1399G=
NM_001145095.3:c.449-1399G= MANE Select NP_001138567.1:n.449-1399G=