Canonical Allele Identifier: CA2718093840
Gene: HHLA1 HGNC NCBI

Linked Data

dbSNP Id: rs145184611

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132091086_132091089dup , CM000670.2:g.132091086_132091089dup GRCh38
NC_000008.10:g.133103333_133103336dup , CM000670.1:g.133103333_133103336dup GRCh37
NC_000008.9:g.133172515_133172518dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000414222.2:c.449-1487_449-1484dup MANE Select ENSP00000388322.1:n.449-1487_449-1484dup
ENST00000673615.1:c.557-1487_557-1484dup ENSP00000500443.1:n.557-1487_557-1484dup
ENST00000414222.1:c.449-1487_449-1484dup ENSP00000388322.1:n.449-1487_449-1484dup
ENST00000434736.6:c.557-1487_557-1484dup ENSP00000407107.2:n.557-1487_557-1484dup
NM_001145095.1:c.449-1487_449-1484dup NP_001138567.1:n.449-1487_449-1484dup
NM_001145095.3:c.449-1487_449-1484dup MANE Select NP_001138567.1:n.449-1487_449-1484dup