Canonical Allele Identifier: CA414400285

Gene: LAMP2

Linked Data

• MyVariant Identifiers: chrX:g.119576465A>T (hg19) ; chrX:g.120442610A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.120442610A>T , CM000685.2:g.120442610A>T	GRCh38
NC_000023.10:g.119576465A>T , CM000685.1:g.119576465A>T	GRCh37
NC_000023.9:g.119460493A>T	NCBI36
NG_007995.1:g.31740T>A , LRG_749:g.31740T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000706600.1:c.917T>A	ENSP00000516464.1:p.Val306Asp
ENST00000200639.9:c.917T>A MANE Select	ENSP00000200639.4:p.Val306Asp
ENST00000200639.8:c.917T>A	ENSP00000200639.4:p.Val306Asp
ENST00000371335.4:c.917T>A	ENSP00000360386.4:p.Val306Asp
ENST00000434600.6:c.917T>A	ENSP00000408411.2:p.Val306Asp
ENST00000486593.5:c.460T>A
NM_001122606.1:c.917T>A , LRG_749t3:c.917T>A	NP_001116078.1:p.Val306Asp
NM_002294.2:c.917T>A , LRG_749t1:c.917T>A	NP_002285.1:p.Val306Asp
NM_013995.2:c.917T>A , LRG_749t2:c.917T>A	NP_054701.1:p.Val306Asp
NM_002294.3:c.917T>A MANE Select	NP_002285.1:p.Val306Asp