Canonical Allele Identifier: CA2454871182

Gene: LAMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.120442570C= , CM000685.2:g.120442570C=	GRCh38
NC_000023.10:g.119576425C= , CM000685.1:g.119576425C=	GRCh37
NC_000023.9:g.119460453C=	NCBI36
NG_007995.1:g.31780G= , LRG_749:g.31780G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000706600.1:c.928+29G=	ENSP00000516464.1:n.928+29G=
ENST00000200639.9:c.928+29G= MANE Select	ENSP00000200639.4:n.928+29G=
ENST00000200639.8:c.928+29G=	ENSP00000200639.4:n.928+29G=
ENST00000371335.4:c.928+29G=	ENSP00000360386.4:n.928+29G=
ENST00000434600.6:c.928+29G=	ENSP00000408411.2:n.928+29G=
ENST00000486593.5:c.471+29G=
NM_001122606.1:c.928+29G= , LRG_749t3:c.928+29G=	NP_001116078.1:n.928+29G=
NM_002294.2:c.928+29G= , LRG_749t1:c.928+29G=	NP_002285.1:n.928+29G=
NM_013995.2:c.928+29G= , LRG_749t2:c.928+29G=	NP_054701.1:n.928+29G=
NM_002294.3:c.928+29G= MANE Select	NP_002285.1:n.928+29G=