Canonical Allele Identifier: CA2668720267

Gene: LAMP3

Linked Data

• gnomAD v4: 3-183152653-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183152653C>A , CM000665.2:g.183152653C>A	GRCh38
NC_000003.11:g.182870441C>A , CM000665.1:g.182870441C>A	GRCh37
NC_000003.10:g.184353135C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265598.8:c.760-150G>T MANE Select	ENSP00000265598.3:n.760-150G>T
ENST00000265598.7:c.760-150G>T	ENSP00000265598.3:n.760-150G>T
ENST00000466939.1:c.688-150G>T	ENSP00000418912.1:n.688-150G>T
NM_014398.3:c.760-150G>T	NP_055213.2:n.760-150G>T
XM_005247360.3:c.760-150G>T	XP_005247417.1:n.760-150G>T
XM_006713586.2:c.688-150G>T	XP_006713649.1:n.688-150G>T
XM_011512688.1:c.760-150G>T	XP_011510990.1:n.760-150G>T
XR_924123.1:n.820-150G>T
XR_924124.1:n.820-150G>T
XM_005247360.5:c.760-150G>T	XP_005247417.1:n.760-150G>T
XM_006713586.3:c.688-150G>T	XP_006713649.1:n.688-150G>T
XM_011512688.2:c.760-150G>T	XP_011510990.1:n.760-150G>T
XM_024453453.1:c.688-150G>T	XP_024309221.1:n.688-150G>T
NM_014398.4:c.760-150G>T MANE Select	NP_055213.2:n.760-150G>T