Canonical Allele Identifier: CA437096177

Gene: LAMP3

Linked Data

• gnomAD v4: 3-183152384-T-C
• MyVariant Identifiers: chr3:g.182870172T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183152384T>C , CM000665.2:g.183152384T>C	GRCh38
NC_000003.11:g.182870172T>C , CM000665.1:g.182870172T>C	GRCh37
NC_000003.10:g.184352866T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265598.8:c.879A>G MANE Select	ENSP00000265598.3:p.Thr293=
ENST00000265598.7:c.879A>G	ENSP00000265598.3:p.Thr293=
ENST00000466939.1:c.807A>G	ENSP00000418912.1:p.Thr269=
NM_014398.3:c.879A>G	NP_055213.2:p.Thr293=
XM_005247360.3:c.879A>G	XP_005247417.1:p.Thr293=
XM_006713586.2:c.807A>G	XP_006713649.1:p.Thr269=
XM_011512688.1:c.879A>G	XP_011510990.1:p.Thr293=
XR_924123.1:n.939A>G
XR_924124.1:n.939A>G
XM_005247360.5:c.879A>G	XP_005247417.1:p.Thr293=
XM_006713586.3:c.807A>G	XP_006713649.1:p.Thr269=
XM_011512688.2:c.879A>G	XP_011510990.1:p.Thr293=
XM_024453453.1:c.807A>G	XP_024309221.1:p.Thr269=
NM_014398.4:c.879A>G MANE Select	NP_055213.2:p.Thr293=