Canonical Allele Identifier: CA2454873138
Gene: LAMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.120449070T= , CM000685.2:g.120449070T= GRCh38
NC_000023.10:g.119582925T= , CM000685.1:g.119582925T= GRCh37
NC_000023.9:g.119466953T= NCBI36
NG_007995.1:g.25280A= , LRG_749:g.25280A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706600.1:c.456A= ENSP00000516464.1:p.Arg152=
ENST00000200639.9:c.456A= MANE Select ENSP00000200639.4:p.Arg152=
ENST00000200639.8:c.456A= ENSP00000200639.4:p.Arg152=
ENST00000371335.4:c.456A= ENSP00000360386.4:p.Arg152=
ENST00000434600.6:c.456A= ENSP00000408411.2:p.Arg152=
NM_001122606.1:c.456A= , LRG_749t3:c.456A= NP_001116078.1:p.Arg152=
NM_002294.2:c.456A= , LRG_749t1:c.456A= NP_002285.1:p.Arg152=
NM_013995.2:c.456A= , LRG_749t2:c.456A= NP_054701.1:p.Arg152=
NM_002294.3:c.456A= MANE Select NP_002285.1:p.Arg152=