Canonical Allele Identifier: CA1425434385

Gene: LAMP3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183152700_183152703delinsAGAG , CM000665.2:g.183152700_183152703delinsAGAG	GRCh38
NC_000003.11:g.182870488_182870491delinsAGAG , CM000665.1:g.182870488_182870491delinsAGAG	GRCh37
NC_000003.10:g.184353182_184353185delinsAGAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265598.8:c.760-200_760-197delinsCTCT MANE Select	ENSP00000265598.3:n.760-200_760-197delinsCTCT
ENST00000265598.7:c.760-200_760-197delinsCTCT	ENSP00000265598.3:n.760-200_760-197delinsCTCT
ENST00000466939.1:c.688-200_688-197delinsCTCT	ENSP00000418912.1:n.688-200_688-197delinsCTCT
NM_014398.3:c.760-200_760-197delinsCTCT	NP_055213.2:n.760-200_760-197delinsCTCT
XM_005247360.3:c.760-200_760-197delinsCTCT	XP_005247417.1:n.760-200_760-197delinsCTCT
XM_006713586.2:c.688-200_688-197delinsCTCT	XP_006713649.1:n.688-200_688-197delinsCTCT
XM_011512688.1:c.760-200_760-197delinsCTCT	XP_011510990.1:n.760-200_760-197delinsCTCT
XR_924123.1:n.820-200_820-197delinsCTCT
XR_924124.1:n.820-200_820-197delinsCTCT
XM_005247360.5:c.760-200_760-197delinsCTCT	XP_005247417.1:n.760-200_760-197delinsCTCT
XM_006713586.3:c.688-200_688-197delinsCTCT	XP_006713649.1:n.688-200_688-197delinsCTCT
XM_011512688.2:c.760-200_760-197delinsCTCT	XP_011510990.1:n.760-200_760-197delinsCTCT
XM_024453453.1:c.688-200_688-197delinsCTCT	XP_024309221.1:n.688-200_688-197delinsCTCT
NM_014398.4:c.760-200_760-197delinsCTCT MANE Select	NP_055213.2:n.760-200_760-197delinsCTCT