Canonical Allele Identifier: CA2823250135

Gene: LAMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.120449213_120449215dup , CM000685.2:g.120449213_120449215dup	GRCh38
NC_000023.10:g.119583068_119583070dup , CM000685.1:g.119583068_119583070dup	GRCh37
NC_000023.9:g.119467096_119467098dup	NCBI36
NG_007995.1:g.25142_25144dup , LRG_749:g.25142_25144dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706600.1:c.398-80_398-78dup	ENSP00000516464.1:n.398-80_398-78dup
ENST00000200639.9:c.398-80_398-78dup MANE Select	ENSP00000200639.4:n.398-80_398-78dup
ENST00000200639.8:c.398-80_398-78dup	ENSP00000200639.4:n.398-80_398-78dup
ENST00000371335.4:c.398-80_398-78dup	ENSP00000360386.4:n.398-80_398-78dup
ENST00000434600.6:c.398-80_398-78dup	ENSP00000408411.2:n.398-80_398-78dup
NM_001122606.1:c.398-80_398-78dup , LRG_749t3:c.398-80_398-78dup	NP_001116078.1:n.398-80_398-78dup
NM_002294.2:c.398-80_398-78dup , LRG_749t1:c.398-80_398-78dup	NP_002285.1:n.398-80_398-78dup
NM_013995.2:c.398-80_398-78dup , LRG_749t2:c.398-80_398-78dup	NP_054701.1:n.398-80_398-78dup
NM_002294.3:c.398-80_398-78dup MANE Select	NP_002285.1:n.398-80_398-78dup