Canonical Allele Identifier: CA2454871212
Gene: LAMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.120442680T= , CM000685.2:g.120442680T= GRCh38
NC_000023.10:g.119576535T= , CM000685.1:g.119576535T= GRCh37
NC_000023.9:g.119460563T= NCBI36
NG_007995.1:g.31670A= , LRG_749:g.31670A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706600.1:c.865-18A= ENSP00000516464.1:n.865-18A=
ENST00000200639.9:c.865-18A= MANE Select ENSP00000200639.4:n.865-18A=
ENST00000200639.8:c.865-18A= ENSP00000200639.4:n.865-18A=
ENST00000371335.4:c.865-18A= ENSP00000360386.4:n.865-18A=
ENST00000434600.6:c.865-18A= ENSP00000408411.2:n.865-18A=
ENST00000486593.5:c.408-18A=
NM_001122606.1:c.865-18A= , LRG_749t3:c.865-18A= NP_001116078.1:n.865-18A=
NM_002294.2:c.865-18A= , LRG_749t1:c.865-18A= NP_002285.1:n.865-18A=
NM_013995.2:c.865-18A= , LRG_749t2:c.865-18A= NP_054701.1:n.865-18A=
NM_002294.3:c.865-18A= MANE Select NP_002285.1:n.865-18A=