Canonical Allele Identifier: CA847613793
Gene: HHLA1 HGNC NCBI

Linked Data

dbSNP Id: rs1351609550
MyVariant Identifiers: chr8:g.133103258del (hg19) chr8:g.132091011del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132091012del , CM000670.2:g.132091012del GRCh38
NC_000008.10:g.133103259del , CM000670.1:g.133103259del GRCh37
NC_000008.9:g.133172441del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000414222.2:c.449-1412del MANE Select ENSP00000388322.1:n.449-1412del
ENST00000673615.1:c.557-1412del ENSP00000500443.1:n.557-1412del
ENST00000414222.1:c.449-1412del ENSP00000388322.1:n.449-1412del
ENST00000434736.6:c.557-1412del ENSP00000407107.2:n.557-1412del
NM_001145095.1:c.449-1412del NP_001138567.1:n.449-1412del
NM_001145095.3:c.449-1412del MANE Select NP_001138567.1:n.449-1412del
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