Canonical Allele Identifier: CA1425434308
Gene: LAMP3 HGNC NCBI

Linked Data

dbSNP Id: rs1720672088

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.183152502dup , CM000665.2:g.183152502dup GRCh38
NC_000003.11:g.182870290dup , CM000665.1:g.182870290dup GRCh37
NC_000003.10:g.184352984dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265598.8:c.766dup MANE Select ENSP00000265598.3:p.Ser256PhefsTer?
ENST00000265598.7:c.766dup ENSP00000265598.3:p.Ser256PhefsTer?
ENST00000466939.1:c.694dup ENSP00000418912.1:p.Ser232PhefsTer?
NM_014398.3:c.766dup NP_055213.2:p.Ser256PhefsTer?
XM_005247360.3:c.766dup XP_005247417.1:p.Ser256PhefsTer?
XM_006713586.2:c.694dup XP_006713649.1:p.Ser232PhefsTer?
XM_011512688.1:c.766dup XP_011510990.1:p.Ser256PhefsTer?
XR_924123.1:n.826dup
XR_924124.1:n.826dup
XM_005247360.5:c.766dup XP_005247417.1:p.Ser256PhefsTer?
XM_006713586.3:c.694dup XP_006713649.1:p.Ser232PhefsTer?
XM_011512688.2:c.766dup XP_011510990.1:p.Ser256PhefsTer?
XM_024453453.1:c.694dup XP_024309221.1:p.Ser232PhefsTer?
NM_014398.4:c.766dup MANE Select NP_055213.2:p.Ser256PhefsTer?