Canonical Allele Identifier: CA2454873145
Gene: LAMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.120449097G= , CM000685.2:g.120449097G= GRCh38
NC_000023.10:g.119582952G= , CM000685.1:g.119582952G= GRCh37
NC_000023.9:g.119466980G= NCBI36
NG_007995.1:g.25253C= , LRG_749:g.25253C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706600.1:c.429C= ENSP00000516464.1:p.Ile143=
ENST00000200639.9:c.429C= MANE Select ENSP00000200639.4:p.Ile143=
ENST00000200639.8:c.429C= ENSP00000200639.4:p.Ile143=
ENST00000371335.4:c.429C= ENSP00000360386.4:p.Ile143=
ENST00000434600.6:c.429C= ENSP00000408411.2:p.Ile143=
NM_001122606.1:c.429C= , LRG_749t3:c.429C= NP_001116078.1:p.Ile143=
NM_002294.2:c.429C= , LRG_749t1:c.429C= NP_002285.1:p.Ile143=
NM_013995.2:c.429C= , LRG_749t2:c.429C= NP_054701.1:p.Ile143=
NM_002294.3:c.429C= MANE Select NP_002285.1:p.Ile143=