Canonical Allele Identifier: CA1820608945

Gene: HHLA1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132090889T= , CM000670.2:g.132090889T=	GRCh38
NC_000008.10:g.133103136T= , CM000670.1:g.133103136T=	GRCh37
NC_000008.9:g.133172318T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000414222.2:c.449-1290A= MANE Select	ENSP00000388322.1:n.449-1290A=
ENST00000673615.1:c.557-1290A=	ENSP00000500443.1:n.557-1290A=
ENST00000414222.1:c.449-1290A=	ENSP00000388322.1:n.449-1290A=
ENST00000434736.6:c.557-1290A=	ENSP00000407107.2:n.557-1290A=
NM_001145095.1:c.449-1290A=	NP_001138567.1:n.449-1290A=
NM_001145095.3:c.449-1290A= MANE Select	NP_001138567.1:n.449-1290A=