Canonical Allele Identifier: CA2454873133
Gene: LAMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.120449059A= , CM000685.2:g.120449059A= GRCh38
NC_000023.10:g.119582914A= , CM000685.1:g.119582914A= GRCh37
NC_000023.9:g.119466942A= NCBI36
NG_007995.1:g.25291T= , LRG_749:g.25291T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706600.1:c.467T= ENSP00000516464.1:p.Leu156=
ENST00000200639.9:c.467T= MANE Select ENSP00000200639.4:p.Leu156=
ENST00000200639.8:c.467T= ENSP00000200639.4:p.Leu156=
ENST00000371335.4:c.467T= ENSP00000360386.4:p.Leu156=
ENST00000434600.6:c.467T= ENSP00000408411.2:p.Leu156=
ENST00000486593.5:c.10T=
NM_001122606.1:c.467T= , LRG_749t3:c.467T= NP_001116078.1:p.Leu156=
NM_002294.2:c.467T= , LRG_749t1:c.467T= NP_002285.1:p.Leu156=
NM_013995.2:c.467T= , LRG_749t2:c.467T= NP_054701.1:p.Leu156=
NM_002294.3:c.467T= MANE Select NP_002285.1:p.Leu156=