Canonical Allele Identifier: CA1425434298

Gene: LAMP3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183152476T= , CM000665.2:g.183152476T=	GRCh38
NC_000003.11:g.182870264T= , CM000665.1:g.182870264T=	GRCh37
NC_000003.10:g.184352958T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265598.8:c.787A= MANE Select	ENSP00000265598.3:p.Ile263=
ENST00000265598.7:c.787A=	ENSP00000265598.3:p.Ile263=
ENST00000466939.1:c.715A=	ENSP00000418912.1:p.Ile239=
NM_014398.3:c.787A=	NP_055213.2:p.Ile263=
XM_005247360.3:c.787A=	XP_005247417.1:p.Ile263=
XM_006713586.2:c.715A=	XP_006713649.1:p.Ile239=
XM_011512688.1:c.787A=	XP_011510990.1:p.Ile263=
XR_924123.1:n.847A=
XR_924124.1:n.847A=
XM_005247360.5:c.787A=	XP_005247417.1:p.Ile263=
XM_006713586.3:c.715A=	XP_006713649.1:p.Ile239=
XM_011512688.2:c.787A=	XP_011510990.1:p.Ile263=
XM_024453453.1:c.715A=	XP_024309221.1:p.Ile239=
NM_014398.4:c.787A= MANE Select	NP_055213.2:p.Ile263=