Canonical Allele Identifier: CA1425434294
Gene: LAMP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.183152472T= , CM000665.2:g.183152472T= GRCh38
NC_000003.11:g.182870260T= , CM000665.1:g.182870260T= GRCh37
NC_000003.10:g.184352954T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265598.8:c.791A= MANE Select ENSP00000265598.3:p.Asp264=
ENST00000265598.7:c.791A= ENSP00000265598.3:p.Asp264=
ENST00000466939.1:c.719A= ENSP00000418912.1:p.Asp240=
NM_014398.3:c.791A= NP_055213.2:p.Asp264=
XM_005247360.3:c.791A= XP_005247417.1:p.Asp264=
XM_006713586.2:c.719A= XP_006713649.1:p.Asp240=
XM_011512688.1:c.791A= XP_011510990.1:p.Asp264=
XR_924123.1:n.851A=
XR_924124.1:n.851A=
XM_005247360.5:c.791A= XP_005247417.1:p.Asp264=
XM_006713586.3:c.719A= XP_006713649.1:p.Asp240=
XM_011512688.2:c.791A= XP_011510990.1:p.Asp264=
XM_024453453.1:c.719A= XP_024309221.1:p.Asp240=
NM_014398.4:c.791A= MANE Select NP_055213.2:p.Asp264=