Canonical Allele Identifier: CA2668720223

Gene: LAMP3

Linked Data

• gnomAD v4: 3-183152631-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183152631_183152632insT , CM000665.2:g.183152631_183152632insT	GRCh38
NC_000003.11:g.182870419_182870420insT , CM000665.1:g.182870419_182870420insT	GRCh37
NC_000003.10:g.184353113_184353114insT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265598.8:c.760-129_760-128insA MANE Select	ENSP00000265598.3:n.760-129_760-128insA
ENST00000265598.7:c.760-129_760-128insA	ENSP00000265598.3:n.760-129_760-128insA
ENST00000466939.1:c.688-129_688-128insA	ENSP00000418912.1:n.688-129_688-128insA
NM_014398.3:c.760-129_760-128insA	NP_055213.2:n.760-129_760-128insA
XM_005247360.3:c.760-129_760-128insA	XP_005247417.1:n.760-129_760-128insA
XM_006713586.2:c.688-129_688-128insA	XP_006713649.1:n.688-129_688-128insA
XM_011512688.1:c.760-129_760-128insA	XP_011510990.1:n.760-129_760-128insA
XR_924123.1:n.820-129_820-128insA
XR_924124.1:n.820-129_820-128insA
XM_005247360.5:c.760-129_760-128insA	XP_005247417.1:n.760-129_760-128insA
XM_006713586.3:c.688-129_688-128insA	XP_006713649.1:n.688-129_688-128insA
XM_011512688.2:c.760-129_760-128insA	XP_011510990.1:n.760-129_760-128insA
XM_024453453.1:c.688-129_688-128insA	XP_024309221.1:n.688-129_688-128insA
NM_014398.4:c.760-129_760-128insA MANE Select	NP_055213.2:n.760-129_760-128insA