Canonical Allele Identifier: CA2454871152

Gene: LAMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.120442478_120442479delinsAC , CM000685.2:g.120442478_120442479delinsAC	GRCh38
NC_000023.10:g.119576333_119576334delinsAC , CM000685.1:g.119576333_119576334delinsAC	GRCh37
NC_000023.9:g.119460361_119460362delinsAC	NCBI36
NG_007995.1:g.31871_31872delinsGT , LRG_749:g.31871_31872delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706600.1:c.928+120_928+121delinsGT	ENSP00000516464.1:n.928+120_928+121delinsGT
ENST00000200639.9:c.928+120_928+121delinsGT MANE Select	ENSP00000200639.4:n.928+120_928+121delinsGT
ENST00000200639.8:c.928+120_928+121delinsGT	ENSP00000200639.4:n.928+120_928+121delinsGT
ENST00000371335.4:c.928+120_928+121delinsGT	ENSP00000360386.4:n.928+120_928+121delinsGT
ENST00000434600.6:c.928+120_928+121delinsGT	ENSP00000408411.2:n.928+120_928+121delinsGT
ENST00000486593.5:c.471+120_471+121delinsGT
NM_001122606.1:c.928+120_928+121delinsGT , LRG_749t3:c.928+120_928+121delinsGT	NP_001116078.1:n.928+120_928+121delinsGT
NM_002294.2:c.928+120_928+121delinsGT , LRG_749t1:c.928+120_928+121delinsGT	NP_002285.1:n.928+120_928+121delinsGT
NM_013995.2:c.928+120_928+121delinsGT , LRG_749t2:c.928+120_928+121delinsGT	NP_054701.1:n.928+120_928+121delinsGT
NM_002294.3:c.928+120_928+121delinsGT MANE Select	NP_002285.1:n.928+120_928+121delinsGT