Canonical Allele Identifier: CA437096163

Gene: LAMP3

Linked Data

• MyVariant Identifiers: chr3:g.182870166G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183152378G>T , CM000665.2:g.183152378G>T	GRCh38
NC_000003.11:g.182870166G>T , CM000665.1:g.182870166G>T	GRCh37
NC_000003.10:g.184352860G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265598.8:c.885C>A MANE Select	ENSP00000265598.3:p.Thr295=
ENST00000265598.7:c.885C>A	ENSP00000265598.3:p.Thr295=
ENST00000466939.1:c.813C>A	ENSP00000418912.1:p.Thr271=
NM_014398.3:c.885C>A	NP_055213.2:p.Thr295=
XM_005247360.3:c.885C>A	XP_005247417.1:p.Thr295=
XM_006713586.2:c.813C>A	XP_006713649.1:p.Thr271=
XM_011512688.1:c.885C>A	XP_011510990.1:p.Thr295=
XR_924123.1:n.945C>A
XR_924124.1:n.945C>A
XM_005247360.5:c.885C>A	XP_005247417.1:p.Thr295=
XM_006713586.3:c.813C>A	XP_006713649.1:p.Thr271=
XM_011512688.2:c.885C>A	XP_011510990.1:p.Thr295=
XM_024453453.1:c.813C>A	XP_024309221.1:p.Thr271=
NM_014398.4:c.885C>A MANE Select	NP_055213.2:p.Thr295=