Canonical Allele Identifier: CA2454879139

Gene: LAMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.120469053C= , CM000685.2:g.120469053C=	GRCh38
NC_000023.10:g.119602908C= , CM000685.1:g.119602908C=	GRCh37
NC_000023.9:g.119486936C=	NCBI36
NG_007995.1:g.5297G= , LRG_749:g.5297G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706600.1:c.64+53G=	ENSP00000516464.1:n.64+53G=
ENST00000200639.9:c.64+53G= MANE Select	ENSP00000200639.4:n.64+53G=
ENST00000200639.8:c.64+53G=	ENSP00000200639.4:n.64+53G=
ENST00000371335.4:c.64+53G=	ENSP00000360386.4:n.64+53G=
ENST00000434600.6:c.64+53G=	ENSP00000408411.2:n.64+53G=
NM_001122606.1:c.64+53G= , LRG_749t3:c.64+53G=	NP_001116078.1:n.64+53G=
NM_002294.2:c.64+53G= , LRG_749t1:c.64+53G=	NP_002285.1:n.64+53G=
NM_013995.2:c.64+53G= , LRG_749t2:c.64+53G=	NP_054701.1:n.64+53G=
NM_002294.3:c.64+53G= MANE Select	NP_002285.1:n.64+53G=