Canonical Allele Identifier: CA2454879203
Gene: LAMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.120469172C= , CM000685.2:g.120469172C= GRCh38
NC_000023.10:g.119603027C= , CM000685.1:g.119603027C= GRCh37
NC_000023.9:g.119487055C= NCBI36
NG_007995.1:g.5178G= , LRG_749:g.5178G=

Transcript Alleles

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