Canonical Allele Identifier: CA2454873111
Gene: LAMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.120448977_120448980delinsGCTC , CM000685.2:g.120448977_120448980delinsGCTC GRCh38
NC_000023.10:g.119582832_119582835delinsGCTC , CM000685.1:g.119582832_119582835delinsGCTC GRCh37
NC_000023.9:g.119466860_119466863delinsGCTC NCBI36
NG_007995.1:g.25370_25373delinsGAGC , LRG_749:g.25370_25373delinsGAGC

Transcript Alleles

HGVS Amino-acid change
ENST00000706600.1:c.546_549delinsGAGC ENSP00000516464.1:p.Val182=
ENST00000200639.9:c.546_549delinsGAGC MANE Select ENSP00000200639.4:p.Val182=
ENST00000200639.8:c.546_549delinsGAGC ENSP00000200639.4:p.Val182=
ENST00000371335.4:c.546_549delinsGAGC ENSP00000360386.4:p.Val182=
ENST00000434600.6:c.546_549delinsGAGC ENSP00000408411.2:p.Val182=
ENST00000486593.5:c.89_92delinsGAGC
NM_001122606.1:c.546_549delinsGAGC , LRG_749t3:c.546_549delinsGAGC NP_001116078.1:p.Val182=
NM_002294.2:c.546_549delinsGAGC , LRG_749t1:c.546_549delinsGAGC NP_002285.1:p.Val182=
NM_013995.2:c.546_549delinsGAGC , LRG_749t2:c.546_549delinsGAGC NP_054701.1:p.Val182=
NM_002294.3:c.546_549delinsGAGC MANE Select NP_002285.1:p.Val182=