Canonical Allele Identifier: CA355321300
Gene: LAMP3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.183152389G>C , CM000665.2:g.183152389G>C GRCh38
NC_000003.11:g.182870177G>C , CM000665.1:g.182870177G>C GRCh37
NC_000003.10:g.184352871G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265598.8:c.874C>G MANE Select ENSP00000265598.3:p.Leu292Val
ENST00000265598.7:c.874C>G ENSP00000265598.3:p.Leu292Val
ENST00000466939.1:c.802C>G ENSP00000418912.1:p.Leu268Val
NM_014398.3:c.874C>G NP_055213.2:p.Leu292Val
XM_005247360.3:c.874C>G XP_005247417.1:p.Leu292Val
XM_006713586.2:c.802C>G XP_006713649.1:p.Leu268Val
XM_011512688.1:c.874C>G XP_011510990.1:p.Leu292Val
XR_924123.1:n.934C>G
XR_924124.1:n.934C>G
XM_005247360.5:c.874C>G XP_005247417.1:p.Leu292Val
XM_006713586.3:c.802C>G XP_006713649.1:p.Leu268Val
XM_011512688.2:c.874C>G XP_011510990.1:p.Leu292Val
XM_024453453.1:c.802C>G XP_024309221.1:p.Leu268Val
NM_014398.4:c.874C>G MANE Select NP_055213.2:p.Leu292Val