Canonical Allele Identifier: CA2454872858
Gene: LAMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.120448016C= , CM000685.2:g.120448016C= GRCh38
NC_000023.10:g.119581871C= , CM000685.1:g.119581871C= GRCh37
NC_000023.9:g.119465899C= NCBI36
NG_007995.1:g.26334G= , LRG_749:g.26334G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706600.1:c.566G= ENSP00000516464.1:p.Cys189=
ENST00000200639.9:c.566G= MANE Select ENSP00000200639.4:p.Cys189=
ENST00000200639.8:c.566G= ENSP00000200639.4:p.Cys189=
ENST00000371335.4:c.566G= ENSP00000360386.4:p.Cys189=
ENST00000434600.6:c.566G= ENSP00000408411.2:p.Cys189=
ENST00000486593.5:c.109G=
NM_001122606.1:c.566G= , LRG_749t3:c.566G= NP_001116078.1:p.Cys189=
NM_002294.2:c.566G= , LRG_749t1:c.566G= NP_002285.1:p.Cys189=
NM_013995.2:c.566G= , LRG_749t2:c.566G= NP_054701.1:p.Cys189=
NM_002294.3:c.566G= MANE Select NP_002285.1:p.Cys189=