Canonical Allele Identifier: CA414401888
Gene: LAMP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.120448988C>T , CM000685.2:g.120448988C>T GRCh38
NC_000023.10:g.119582843C>T , CM000685.1:g.119582843C>T GRCh37
NC_000023.9:g.119466871C>T NCBI36
NG_007995.1:g.25362G>A , LRG_749:g.25362G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000706600.1:c.538G>A ENSP00000516464.1:p.Gly180Ser
ENST00000200639.9:c.538G>A MANE Select ENSP00000200639.4:p.Gly180Ser
ENST00000200639.8:c.538G>A ENSP00000200639.4:p.Gly180Ser
ENST00000371335.4:c.538G>A ENSP00000360386.4:p.Gly180Ser
ENST00000434600.6:c.538G>A ENSP00000408411.2:p.Gly180Ser
ENST00000486593.5:c.81G>A
NM_001122606.1:c.538G>A , LRG_749t3:c.538G>A NP_001116078.1:p.Gly180Ser
NM_002294.2:c.538G>A , LRG_749t1:c.538G>A NP_002285.1:p.Gly180Ser
NM_013995.2:c.538G>A , LRG_749t2:c.538G>A NP_054701.1:p.Gly180Ser
NM_002294.3:c.538G>A MANE Select NP_002285.1:p.Gly180Ser