Canonical Allele Identifier: CA1820608917

Gene: HHLA1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132090865_132090868delinsTCTC , CM000670.2:g.132090865_132090868delinsTCTC	GRCh38
NC_000008.10:g.133103112_133103115delinsTCTC , CM000670.1:g.133103112_133103115delinsTCTC	GRCh37
NC_000008.9:g.133172294_133172297delinsTCTC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000414222.2:c.449-1269_449-1266delinsGAGA MANE Select	ENSP00000388322.1:n.449-1269_449-1266delinsGAGA
ENST00000673615.1:c.557-1269_557-1266delinsGAGA	ENSP00000500443.1:n.557-1269_557-1266delinsGAGA
ENST00000414222.1:c.449-1269_449-1266delinsGAGA	ENSP00000388322.1:n.449-1269_449-1266delinsGAGA
ENST00000434736.6:c.557-1269_557-1266delinsGAGA	ENSP00000407107.2:n.557-1269_557-1266delinsGAGA
NM_001145095.1:c.449-1269_449-1266delinsGAGA	NP_001138567.1:n.449-1269_449-1266delinsGAGA
NM_001145095.3:c.449-1269_449-1266delinsGAGA MANE Select	NP_001138567.1:n.449-1269_449-1266delinsGAGA