Canonical Allele Identifier: CA2454879221
Gene: LAMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.120469196G= , CM000685.2:g.120469196G= GRCh38
NC_000023.10:g.119603051G= , CM000685.1:g.119603051G= GRCh37
NC_000023.9:g.119487079G= NCBI36
NG_007995.1:g.5154C= , LRG_749:g.5154C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706600.1:c.-27C= ENSP00000516464.1:n.-27C=
ENST00000200639.9:c.-27C= MANE Select ENSP00000200639.4:n.-27C=
ENST00000200639.8:c.-27C= ENSP00000200639.4:n.-27C=
ENST00000371335.4:c.-27C= ENSP00000360386.4:n.-27C=
ENST00000434600.6:c.-27C= ENSP00000408411.2:n.-27C=
NM_001122606.1:c.-27C= , LRG_749t3:c.-27C= NP_001116078.1:n.-27C=
NM_002294.2:c.-27C= , LRG_749t1:c.-27C= NP_002285.1:n.-27C=
NM_013995.2:c.-27C= , LRG_749t2:c.-27C= NP_054701.1:n.-27C=
NM_002294.3:c.-27C= MANE Select NP_002285.1:n.-27C=