Canonical Allele Identifier: CA2668720156
Gene: LAMP3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.183152575del , CM000665.2:g.183152575del GRCh38
NC_000003.11:g.182870363del , CM000665.1:g.182870363del GRCh37
NC_000003.10:g.184353057del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265598.8:c.760-71del MANE Select ENSP00000265598.3:n.760-71del
ENST00000265598.7:c.760-71del ENSP00000265598.3:n.760-71del
ENST00000466939.1:c.688-71del ENSP00000418912.1:n.688-71del
NM_014398.3:c.760-71del NP_055213.2:n.760-71del
XM_005247360.3:c.760-71del XP_005247417.1:n.760-71del
XM_006713586.2:c.688-71del XP_006713649.1:n.688-71del
XM_011512688.1:c.760-71del XP_011510990.1:n.760-71del
XR_924123.1:n.820-71del
XR_924124.1:n.820-71del
XM_005247360.5:c.760-71del XP_005247417.1:n.760-71del
XM_006713586.3:c.688-71del XP_006713649.1:n.688-71del
XM_011512688.2:c.760-71del XP_011510990.1:n.760-71del
XM_024453453.1:c.688-71del XP_024309221.1:n.688-71del
NM_014398.4:c.760-71del MANE Select NP_055213.2:n.760-71del