Canonical Allele Identifier: CA1425434262

Gene: LAMP3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183152402G= , CM000665.2:g.183152402G=	GRCh38
NC_000003.11:g.182870190G= , CM000665.1:g.182870190G=	GRCh37
NC_000003.10:g.184352884G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265598.8:c.861C= MANE Select	ENSP00000265598.3:p.Gly287=
ENST00000265598.7:c.861C=	ENSP00000265598.3:p.Gly287=
ENST00000466939.1:c.789C=	ENSP00000418912.1:p.Gly263=
NM_014398.3:c.861C=	NP_055213.2:p.Gly287=
XM_005247360.3:c.861C=	XP_005247417.1:p.Gly287=
XM_006713586.2:c.789C=	XP_006713649.1:p.Gly263=
XM_011512688.1:c.861C=	XP_011510990.1:p.Gly287=
XR_924123.1:n.921C=
XR_924124.1:n.921C=
XM_005247360.5:c.861C=	XP_005247417.1:p.Gly287=
XM_006713586.3:c.789C=	XP_006713649.1:p.Gly263=
XM_011512688.2:c.861C=	XP_011510990.1:p.Gly287=
XM_024453453.1:c.789C=	XP_024309221.1:p.Gly263=
NM_014398.4:c.861C= MANE Select	NP_055213.2:p.Gly287=