Canonical Allele Identifier: CA355321286

Gene: LAMP3

Linked Data

• MyVariant Identifiers: chr3:g.182870170A>C (hg19) ; chr3:g.183152382A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183152382A>C , CM000665.2:g.183152382A>C	GRCh38
NC_000003.11:g.182870170A>C , CM000665.1:g.182870170A>C	GRCh37
NC_000003.10:g.184352864A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265598.8:c.881T>G MANE Select	ENSP00000265598.3:p.Phe294Cys
ENST00000265598.7:c.881T>G	ENSP00000265598.3:p.Phe294Cys
ENST00000466939.1:c.809T>G	ENSP00000418912.1:p.Phe270Cys
NM_014398.3:c.881T>G	NP_055213.2:p.Phe294Cys
XM_005247360.3:c.881T>G	XP_005247417.1:p.Phe294Cys
XM_006713586.2:c.809T>G	XP_006713649.1:p.Phe270Cys
XM_011512688.1:c.881T>G	XP_011510990.1:p.Phe294Cys
XR_924123.1:n.941T>G
XR_924124.1:n.941T>G
XM_005247360.5:c.881T>G	XP_005247417.1:p.Phe294Cys
XM_006713586.3:c.809T>G	XP_006713649.1:p.Phe270Cys
XM_011512688.2:c.881T>G	XP_011510990.1:p.Phe294Cys
XM_024453453.1:c.809T>G	XP_024309221.1:p.Phe270Cys
NM_014398.4:c.881T>G MANE Select	NP_055213.2:p.Phe294Cys