Canonical Allele Identifier: CA1425434392
Gene: LAMP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.183152731G= , CM000665.2:g.183152731G= GRCh38
NC_000003.11:g.182870519G= , CM000665.1:g.182870519G= GRCh37
NC_000003.10:g.184353213G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265598.8:c.760-228C= MANE Select ENSP00000265598.3:n.760-228C=
ENST00000265598.7:c.760-228C= ENSP00000265598.3:n.760-228C=
ENST00000466939.1:c.688-228C= ENSP00000418912.1:n.688-228C=
NM_014398.3:c.760-228C= NP_055213.2:n.760-228C=
XM_005247360.3:c.760-228C= XP_005247417.1:n.760-228C=
XM_006713586.2:c.688-228C= XP_006713649.1:n.688-228C=
XM_011512688.1:c.760-228C= XP_011510990.1:n.760-228C=
XR_924123.1:n.820-228C=
XR_924124.1:n.820-228C=
XM_005247360.5:c.760-228C= XP_005247417.1:n.760-228C=
XM_006713586.3:c.688-228C= XP_006713649.1:n.688-228C=
XM_011512688.2:c.760-228C= XP_011510990.1:n.760-228C=
XM_024453453.1:c.688-228C= XP_024309221.1:n.688-228C=
NM_014398.4:c.760-228C= MANE Select NP_055213.2:n.760-228C=