Canonical Allele Identifier: CA183779
Gene: LAMP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 179126
ClinVar RCV Id: RCV000155911
dbSNP Id: rs727504648

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.120446318_120446319del , CM000685.2:g.120446318_120446319del GRCh38
NC_000023.10:g.119580173_119580174del , CM000685.1:g.119580173_119580174del GRCh37
NC_000023.9:g.119464201_119464202del NCBI36
NG_007995.1:g.28032_28033del , LRG_749:g.28032_28033del

Transcript Alleles

HGVS Amino-acid change
ENST00000706600.1:c.851_852del ENSP00000516464.1:p.Phe284CysfsTer7
ENST00000200639.9:c.851_852del MANE Select ENSP00000200639.4:p.Phe284CysfsTer7
ENST00000200639.8:c.851_852del ENSP00000200639.4:p.Phe284CysfsTer7
ENST00000371335.4:c.851_852del ENSP00000360386.4:p.Phe284CysfsTer7
ENST00000434600.6:c.851_852del ENSP00000408411.2:p.Phe284CysfsTer7
ENST00000486593.5:c.394_395del
NM_001122606.1:c.851_852del , LRG_749t3:c.851_852del NP_001116078.1:p.Phe284CysfsTer7
NM_002294.2:c.851_852del , LRG_749t1:c.851_852del NP_002285.1:p.Phe284CysfsTer7
NM_013995.2:c.851_852del , LRG_749t2:c.851_852del NP_054701.1:p.Phe284CysfsTer7
NM_002294.3:c.851_852del MANE Select NP_002285.1:p.Phe284CysfsTer7