Canonical Allele Identifier: CA1820609017
Gene: HHLA1 HGNC NCBI

Linked Data

dbSNP Id: rs1823937640

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132090960_132090963del , CM000670.2:g.132090960_132090963del GRCh38
NC_000008.10:g.133103207_133103210del , CM000670.1:g.133103207_133103210del GRCh37
NC_000008.9:g.133172389_133172392del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000414222.2:c.449-1364_449-1361del MANE Select ENSP00000388322.1:n.449-1364_449-1361del
ENST00000673615.1:c.557-1364_557-1361del ENSP00000500443.1:n.557-1364_557-1361del
ENST00000414222.1:c.449-1364_449-1361del ENSP00000388322.1:n.449-1364_449-1361del
ENST00000434736.6:c.557-1364_557-1361del ENSP00000407107.2:n.557-1364_557-1361del
NM_001145095.1:c.449-1364_449-1361del NP_001138567.1:n.449-1364_449-1361del
NM_001145095.3:c.449-1364_449-1361del MANE Select NP_001138567.1:n.449-1364_449-1361del