Canonical Allele Identifier: CA2454873122

Gene: LAMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.120449022G= , CM000685.2:g.120449022G=	GRCh38
NC_000023.10:g.119582877G= , CM000685.1:g.119582877G=	GRCh37
NC_000023.9:g.119466905G=	NCBI36
NG_007995.1:g.25328C= , LRG_749:g.25328C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706600.1:c.504C=	ENSP00000516464.1:p.Tyr168=
ENST00000200639.9:c.504C= MANE Select	ENSP00000200639.4:p.Tyr168=
ENST00000200639.8:c.504C=	ENSP00000200639.4:p.Tyr168=
ENST00000371335.4:c.504C=	ENSP00000360386.4:p.Tyr168=
ENST00000434600.6:c.504C=	ENSP00000408411.2:p.Tyr168=
ENST00000486593.5:c.47C=
NM_001122606.1:c.504C= , LRG_749t3:c.504C=	NP_001116078.1:p.Tyr168=
NM_002294.2:c.504C= , LRG_749t1:c.504C=	NP_002285.1:p.Tyr168=
NM_013995.2:c.504C= , LRG_749t2:c.504C=	NP_054701.1:p.Tyr168=
NM_002294.3:c.504C= MANE Select	NP_002285.1:p.Tyr168=