Canonical Allele Identifier: CA414402055
Gene: LAMP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.120449033C>A , CM000685.2:g.120449033C>A GRCh38
NC_000023.10:g.119582888C>A , CM000685.1:g.119582888C>A GRCh37
NC_000023.9:g.119466916C>A NCBI36
NG_007995.1:g.25317G>T , LRG_749:g.25317G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706600.1:c.493G>T ENSP00000516464.1:p.Val165Phe
ENST00000200639.9:c.493G>T MANE Select ENSP00000200639.4:p.Val165Phe
ENST00000200639.8:c.493G>T ENSP00000200639.4:p.Val165Phe
ENST00000371335.4:c.493G>T ENSP00000360386.4:p.Val165Phe
ENST00000434600.6:c.493G>T ENSP00000408411.2:p.Val165Phe
ENST00000486593.5:c.36G>T
NM_001122606.1:c.493G>T , LRG_749t3:c.493G>T NP_001116078.1:p.Val165Phe
NM_002294.2:c.493G>T , LRG_749t1:c.493G>T NP_002285.1:p.Val165Phe
NM_013995.2:c.493G>T , LRG_749t2:c.493G>T NP_054701.1:p.Val165Phe
NM_002294.3:c.493G>T MANE Select NP_002285.1:p.Val165Phe