Canonical Allele Identifier: CA1425434417
Gene: LAMP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.183152783_183152784delinsTG , CM000665.2:g.183152783_183152784delinsTG GRCh38
NC_000003.11:g.182870571_182870572delinsTG , CM000665.1:g.182870571_182870572delinsTG GRCh37
NC_000003.10:g.184353265_184353266delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265598.8:c.760-281_760-280delinsCA MANE Select ENSP00000265598.3:n.760-281_760-280delinsCA
ENST00000265598.7:c.760-281_760-280delinsCA ENSP00000265598.3:n.760-281_760-280delinsCA
ENST00000466939.1:c.688-281_688-280delinsCA ENSP00000418912.1:n.688-281_688-280delinsCA
NM_014398.3:c.760-281_760-280delinsCA NP_055213.2:n.760-281_760-280delinsCA
XM_005247360.3:c.760-281_760-280delinsCA XP_005247417.1:n.760-281_760-280delinsCA
XM_006713586.2:c.688-281_688-280delinsCA XP_006713649.1:n.688-281_688-280delinsCA
XM_011512688.1:c.760-281_760-280delinsCA XP_011510990.1:n.760-281_760-280delinsCA
XR_924123.1:n.820-281_820-280delinsCA
XR_924124.1:n.820-281_820-280delinsCA
XM_005247360.5:c.760-281_760-280delinsCA XP_005247417.1:n.760-281_760-280delinsCA
XM_006713586.3:c.688-281_688-280delinsCA XP_006713649.1:n.688-281_688-280delinsCA
XM_011512688.2:c.760-281_760-280delinsCA XP_011510990.1:n.760-281_760-280delinsCA
XM_024453453.1:c.688-281_688-280delinsCA XP_024309221.1:n.688-281_688-280delinsCA
NM_014398.4:c.760-281_760-280delinsCA MANE Select NP_055213.2:n.760-281_760-280delinsCA