Canonical Allele Identifier: CA437096182

Gene: LAMP3

Linked Data

• MyVariant Identifiers: chr3:g.182870175G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183152387G>T , CM000665.2:g.183152387G>T	GRCh38
NC_000003.11:g.182870175G>T , CM000665.1:g.182870175G>T	GRCh37
NC_000003.10:g.184352869G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265598.8:c.876C>A MANE Select	ENSP00000265598.3:p.Leu292=
ENST00000265598.7:c.876C>A	ENSP00000265598.3:p.Leu292=
ENST00000466939.1:c.804C>A	ENSP00000418912.1:p.Leu268=
NM_014398.3:c.876C>A	NP_055213.2:p.Leu292=
XM_005247360.3:c.876C>A	XP_005247417.1:p.Leu292=
XM_006713586.2:c.804C>A	XP_006713649.1:p.Leu268=
XM_011512688.1:c.876C>A	XP_011510990.1:p.Leu292=
XR_924123.1:n.936C>A
XR_924124.1:n.936C>A
XM_005247360.5:c.876C>A	XP_005247417.1:p.Leu292=
XM_006713586.3:c.804C>A	XP_006713649.1:p.Leu268=
XM_011512688.2:c.876C>A	XP_011510990.1:p.Leu292=
XM_024453453.1:c.804C>A	XP_024309221.1:p.Leu268=
NM_014398.4:c.876C>A MANE Select	NP_055213.2:p.Leu292=