Canonical Allele Identifier: CA2694598216

Gene: LAMP2

Linked Data

• gnomAD v4: X-120448094-ACC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.120448095_120448096del , CM000685.2:g.120448095_120448096del	GRCh38
NC_000023.10:g.119581950_119581951del , CM000685.1:g.119581950_119581951del	GRCh37
NC_000023.9:g.119465978_119465979del	NCBI36
NG_007995.1:g.26254_26255del , LRG_749:g.26254_26255del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706600.1:c.557-71_557-70del	ENSP00000516464.1:n.557-71_557-70del
ENST00000200639.9:c.557-71_557-70del MANE Select	ENSP00000200639.4:n.557-71_557-70del
ENST00000200639.8:c.557-71_557-70del	ENSP00000200639.4:n.557-71_557-70del
ENST00000371335.4:c.557-71_557-70del	ENSP00000360386.4:n.557-71_557-70del
ENST00000434600.6:c.557-71_557-70del	ENSP00000408411.2:n.557-71_557-70del
ENST00000486593.5:c.100-71_100-70del
NM_001122606.1:c.557-71_557-70del , LRG_749t3:c.557-71_557-70del	NP_001116078.1:n.557-71_557-70del
NM_002294.2:c.557-71_557-70del , LRG_749t1:c.557-71_557-70del	NP_002285.1:n.557-71_557-70del
NM_013995.2:c.557-71_557-70del , LRG_749t2:c.557-71_557-70del	NP_054701.1:n.557-71_557-70del
NM_002294.3:c.557-71_557-70del MANE Select	NP_002285.1:n.557-71_557-70del