Canonical Allele Identifier: CA1057153689

Gene: LAMP3

Linked Data

• dbSNP Id: rs1720674521
• gnomAD v3: 3-183152554-G-GC
• gnomAD v4: 3-183152554-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183152555dup , CM000665.2:g.183152555dup	GRCh38
NC_000003.11:g.182870343dup , CM000665.1:g.182870343dup	GRCh37
NC_000003.10:g.184353037dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265598.8:c.760-52dup MANE Select	ENSP00000265598.3:n.760-52dup
ENST00000265598.7:c.760-52dup	ENSP00000265598.3:n.760-52dup
ENST00000466939.1:c.688-52dup	ENSP00000418912.1:n.688-52dup
NM_014398.3:c.760-52dup	NP_055213.2:n.760-52dup
XM_005247360.3:c.760-52dup	XP_005247417.1:n.760-52dup
XM_006713586.2:c.688-52dup	XP_006713649.1:n.688-52dup
XM_011512688.1:c.760-52dup	XP_011510990.1:n.760-52dup
XR_924123.1:n.820-52dup
XR_924124.1:n.820-52dup
XM_005247360.5:c.760-52dup	XP_005247417.1:n.760-52dup
XM_006713586.3:c.688-52dup	XP_006713649.1:n.688-52dup
XM_011512688.2:c.760-52dup	XP_011510990.1:n.760-52dup
XM_024453453.1:c.688-52dup	XP_024309221.1:n.688-52dup
NM_014398.4:c.760-52dup MANE Select	NP_055213.2:n.760-52dup