Canonical Allele Identifier: CA2454873140
Gene: LAMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.120449073A= , CM000685.2:g.120449073A= GRCh38
NC_000023.10:g.119582928A= , CM000685.1:g.119582928A= GRCh37
NC_000023.9:g.119466956A= NCBI36
NG_007995.1:g.25277T= , LRG_749:g.25277T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706600.1:c.453T= ENSP00000516464.1:p.Phe151=
ENST00000200639.9:c.453T= MANE Select ENSP00000200639.4:p.Phe151=
ENST00000200639.8:c.453T= ENSP00000200639.4:p.Phe151=
ENST00000371335.4:c.453T= ENSP00000360386.4:p.Phe151=
ENST00000434600.6:c.453T= ENSP00000408411.2:p.Phe151=
NM_001122606.1:c.453T= , LRG_749t3:c.453T= NP_001116078.1:p.Phe151=
NM_002294.2:c.453T= , LRG_749t1:c.453T= NP_002285.1:p.Phe151=
NM_013995.2:c.453T= , LRG_749t2:c.453T= NP_054701.1:p.Phe151=
NM_002294.3:c.453T= MANE Select NP_002285.1:p.Phe151=