Canonical Allele Identifier: CA1820609016

Gene: HHLA1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132090959_132090963delinsCCGTG , CM000670.2:g.132090959_132090963delinsCCGTG	GRCh38
NC_000008.10:g.133103206_133103210delinsCCGTG , CM000670.1:g.133103206_133103210delinsCCGTG	GRCh37
NC_000008.9:g.133172388_133172392delinsCCGTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000414222.2:c.449-1364_449-1360delinsCACGG MANE Select	ENSP00000388322.1:n.449-1364_449-1360delinsCACGG
ENST00000673615.1:c.557-1364_557-1360delinsCACGG	ENSP00000500443.1:n.557-1364_557-1360delinsCACGG
ENST00000414222.1:c.449-1364_449-1360delinsCACGG	ENSP00000388322.1:n.449-1364_449-1360delinsCACGG
ENST00000434736.6:c.557-1364_557-1360delinsCACGG	ENSP00000407107.2:n.557-1364_557-1360delinsCACGG
NM_001145095.1:c.449-1364_449-1360delinsCACGG	NP_001138567.1:n.449-1364_449-1360delinsCACGG
NM_001145095.3:c.449-1364_449-1360delinsCACGG MANE Select	NP_001138567.1:n.449-1364_449-1360delinsCACGG