Canonical Allele Identifier: CA355321347
Gene: LAMP3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.183152411A>T , CM000665.2:g.183152411A>T GRCh38
NC_000003.11:g.182870199A>T , CM000665.1:g.182870199A>T GRCh37
NC_000003.10:g.184352893A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265598.8:c.852T>A MANE Select ENSP00000265598.3:p.Asn284Lys
ENST00000265598.7:c.852T>A ENSP00000265598.3:p.Asn284Lys
ENST00000466939.1:c.780T>A ENSP00000418912.1:p.Asn260Lys
NM_014398.3:c.852T>A NP_055213.2:p.Asn284Lys
XM_005247360.3:c.852T>A XP_005247417.1:p.Asn284Lys
XM_006713586.2:c.780T>A XP_006713649.1:p.Asn260Lys
XM_011512688.1:c.852T>A XP_011510990.1:p.Asn284Lys
XR_924123.1:n.912T>A
XR_924124.1:n.912T>A
XM_005247360.5:c.852T>A XP_005247417.1:p.Asn284Lys
XM_006713586.3:c.780T>A XP_006713649.1:p.Asn260Lys
XM_011512688.2:c.852T>A XP_011510990.1:p.Asn284Lys
XM_024453453.1:c.780T>A XP_024309221.1:p.Asn260Lys
NM_014398.4:c.852T>A MANE Select NP_055213.2:p.Asn284Lys