Canonical Allele Identifier: CA2739015265

Gene: LAMP2

Linked Data

• dbSNP Id: rs2147295013

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.120469212del , CM000685.2:g.120469212del	GRCh38
NC_000023.10:g.119603067del , CM000685.1:g.119603067del	GRCh37
NC_000023.9:g.119487095del	NCBI36
NG_007995.1:g.5138del , LRG_749:g.5138del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706600.1:c.-43del	ENSP00000516464.1:n.-43del
ENST00000200639.9:c.-43del MANE Select	ENSP00000200639.4:n.-43del
ENST00000200639.8:c.-43del	ENSP00000200639.4:n.-43del
ENST00000371335.4:c.-43del	ENSP00000360386.4:n.-43del
ENST00000434600.6:c.-43del	ENSP00000408411.2:n.-43del
NM_001122606.1:c.-43del , LRG_749t3:c.-43del	NP_001116078.1:n.-43del
NM_002294.2:c.-43del , LRG_749t1:c.-43del	NP_002285.1:n.-43del
NM_013995.2:c.-43del , LRG_749t2:c.-43del	NP_054701.1:n.-43del
NM_002294.3:c.-43del MANE Select	NP_002285.1:n.-43del