Canonical Allele Identifier: CA2454873174
Gene: LAMP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.120449200T= , CM000685.2:g.120449200T= GRCh38
NC_000023.10:g.119583055T= , CM000685.1:g.119583055T= GRCh37
NC_000023.9:g.119467083T= NCBI36
NG_007995.1:g.25150A= , LRG_749:g.25150A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706600.1:c.398-72A= ENSP00000516464.1:n.398-72A=
ENST00000200639.9:c.398-72A= MANE Select ENSP00000200639.4:n.398-72A=
ENST00000200639.8:c.398-72A= ENSP00000200639.4:n.398-72A=
ENST00000371335.4:c.398-72A= ENSP00000360386.4:n.398-72A=
ENST00000434600.6:c.398-72A= ENSP00000408411.2:n.398-72A=
NM_001122606.1:c.398-72A= , LRG_749t3:c.398-72A= NP_001116078.1:n.398-72A=
NM_002294.2:c.398-72A= , LRG_749t1:c.398-72A= NP_002285.1:n.398-72A=
NM_013995.2:c.398-72A= , LRG_749t2:c.398-72A= NP_054701.1:n.398-72A=
NM_002294.3:c.398-72A= MANE Select NP_002285.1:n.398-72A=
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