Canonical Allele Identifier: CA2454873129
Gene: LAMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.120449043C= , CM000685.2:g.120449043C= GRCh38
NC_000023.10:g.119582898C= , CM000685.1:g.119582898C= GRCh37
NC_000023.9:g.119466926C= NCBI36
NG_007995.1:g.25307G= , LRG_749:g.25307G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706600.1:c.483G= ENSP00000516464.1:p.Lys161=
ENST00000200639.9:c.483G= MANE Select ENSP00000200639.4:p.Lys161=
ENST00000200639.8:c.483G= ENSP00000200639.4:p.Lys161=
ENST00000371335.4:c.483G= ENSP00000360386.4:p.Lys161=
ENST00000434600.6:c.483G= ENSP00000408411.2:p.Lys161=
ENST00000486593.5:c.26G=
NM_001122606.1:c.483G= , LRG_749t3:c.483G= NP_001116078.1:p.Lys161=
NM_002294.2:c.483G= , LRG_749t1:c.483G= NP_002285.1:p.Lys161=
NM_013995.2:c.483G= , LRG_749t2:c.483G= NP_054701.1:p.Lys161=
NM_002294.3:c.483G= MANE Select NP_002285.1:p.Lys161=