Canonical Allele Identifier: CA1820609012
Gene: HHLA1 HGNC NCBI

Linked Data

dbSNP Id: rs1823937562

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132090957_132090958insTCT , CM000670.2:g.132090957_132090958insTCT GRCh38
NC_000008.10:g.133103204_133103205insTCT , CM000670.1:g.133103204_133103205insTCT GRCh37
NC_000008.9:g.133172386_133172387insTCT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000414222.2:c.449-1359_449-1358insAGA MANE Select ENSP00000388322.1:n.449-1359_449-1358insA...
ENST00000673615.1:c.557-1359_557-1358insAGA ENSP00000500443.1:n.557-1359_557-1358insA...
ENST00000414222.1:c.449-1359_449-1358insAGA ENSP00000388322.1:n.449-1359_449-1358insA...
ENST00000434736.6:c.557-1359_557-1358insAGA ENSP00000407107.2:n.557-1359_557-1358insA...
NM_001145095.1:c.449-1359_449-1358insAGA NP_001138567.1:n.449-1359_449-1358insAGA
NM_001145095.3:c.449-1359_449-1358insAGA MANE Select NP_001138567.1:n.449-1359_449-1358insAGA