Canonical Allele Identifier: CA2454872269
Gene: LAMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.120446304C= , CM000685.2:g.120446304C= GRCh38
NC_000023.10:g.119580159C= , CM000685.1:g.119580159C= GRCh37
NC_000023.9:g.119464187C= NCBI36
NG_007995.1:g.28046G= , LRG_749:g.28046G=

Transcript Alleles

HGVS Amino-acid Change
NM_002294.3:c.864+1G= MANE Select NP_002285.1:n.864+1G=
ENST00000200639.9:c.864+1G= MANE Select ENSP00000200639.4:n.864+1G=
NM_001122606.1:c.864+1G= , LRG_749t3:c.864+1G= NP_001116078.1:n.864+1G=
NM_002294.2:c.864+1G= , LRG_749t1:c.864+1G= NP_002285.1:n.864+1G=
NM_013995.2:c.864+1G= , LRG_749t2:c.864+1G= NP_054701.1:n.864+1G=
ENST00000200639.8:c.864+1G= ENSP00000200639.4:n.864+1G=
ENST00000371335.4:c.864+1G= ENSP00000360386.4:n.864+1G=
ENST00000434600.6:c.864+1G= ENSP00000408411.2:n.864+1G=
ENST00000486593.5:c.407+1G=
ENST00000706600.1:c.864+1G= ENSP00000516464.1:n.864+1G=