Canonical Allele Identifier: CA2454879229
Gene: LAMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.120469210_120469213delinsTACA , CM000685.2:g.120469210_120469213delinsTACA GRCh38
NC_000023.10:g.119603065_119603068delinsTACA , CM000685.1:g.119603065_119603068delinsTACA GRCh37
NC_000023.9:g.119487093_119487096delinsTACA NCBI36
NG_007995.1:g.5137_5140delinsTGTA , LRG_749:g.5137_5140delinsTGTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000706600.1:c.-44_-41delinsTGTA ENSP00000516464.1:n.-44_-41delinsTGTA
ENST00000200639.9:c.-44_-41delinsTGTA MANE Select ENSP00000200639.4:n.-44_-41delinsTGTA
ENST00000200639.8:c.-44_-41delinsTGTA ENSP00000200639.4:n.-44_-41delinsTGTA
ENST00000371335.4:c.-44_-41delinsTGTA ENSP00000360386.4:n.-44_-41delinsTGTA
ENST00000434600.6:c.-44_-41delinsTGTA ENSP00000408411.2:n.-44_-41delinsTGTA
NM_001122606.1:c.-44_-41delinsTGTA , LRG_749t3:c.-44_-41delinsTGTA NP_001116078.1:n.-44_-41delinsTGTA
NM_002294.2:c.-44_-41delinsTGTA , LRG_749t1:c.-44_-41delinsTGTA NP_002285.1:n.-44_-41delinsTGTA
NM_013995.2:c.-44_-41delinsTGTA , LRG_749t2:c.-44_-41delinsTGTA NP_054701.1:n.-44_-41delinsTGTA
NM_002294.3:c.-44_-41delinsTGTA MANE Select NP_002285.1:n.-44_-41delinsTGTA