Canonical Allele Identifier: CA1425434255

Gene: LAMP3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183152380T= , CM000665.2:g.183152380T=	GRCh38
NC_000003.11:g.182870168T= , CM000665.1:g.182870168T=	GRCh37
NC_000003.10:g.184352862T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265598.8:c.883A= MANE Select	ENSP00000265598.3:p.Thr295=
ENST00000265598.7:c.883A=	ENSP00000265598.3:p.Thr295=
ENST00000466939.1:c.811A=	ENSP00000418912.1:p.Thr271=
NM_014398.3:c.883A=	NP_055213.2:p.Thr295=
XM_005247360.3:c.883A=	XP_005247417.1:p.Thr295=
XM_006713586.2:c.811A=	XP_006713649.1:p.Thr271=
XM_011512688.1:c.883A=	XP_011510990.1:p.Thr295=
XR_924123.1:n.943A=
XR_924124.1:n.943A=
XM_005247360.5:c.883A=	XP_005247417.1:p.Thr295=
XM_006713586.3:c.811A=	XP_006713649.1:p.Thr271=
XM_011512688.2:c.883A=	XP_011510990.1:p.Thr295=
XM_024453453.1:c.811A=	XP_024309221.1:p.Thr271=
NM_014398.4:c.883A= MANE Select	NP_055213.2:p.Thr295=