Canonical Allele Identifier: CA355321558

Gene: LAMP3

Linked Data

• MyVariant Identifiers: chr3:g.182870282G>C (hg19) ; chr3:g.183152494G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183152494G>C , CM000665.2:g.183152494G>C	GRCh38
NC_000003.11:g.182870282G>C , CM000665.1:g.182870282G>C	GRCh37
NC_000003.10:g.184352976G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265598.8:c.769C>G MANE Select	ENSP00000265598.3:p.Pro257Ala
ENST00000265598.7:c.769C>G	ENSP00000265598.3:p.Pro257Ala
ENST00000466939.1:c.697C>G	ENSP00000418912.1:p.Pro233Ala
NM_014398.3:c.769C>G	NP_055213.2:p.Pro257Ala
XM_005247360.3:c.769C>G	XP_005247417.1:p.Pro257Ala
XM_006713586.2:c.697C>G	XP_006713649.1:p.Pro233Ala
XM_011512688.1:c.769C>G	XP_011510990.1:p.Pro257Ala
XR_924123.1:n.829C>G
XR_924124.1:n.829C>G
XM_005247360.5:c.769C>G	XP_005247417.1:p.Pro257Ala
XM_006713586.3:c.697C>G	XP_006713649.1:p.Pro233Ala
XM_011512688.2:c.769C>G	XP_011510990.1:p.Pro257Ala
XM_024453453.1:c.697C>G	XP_024309221.1:p.Pro233Ala
NM_014398.4:c.769C>G MANE Select	NP_055213.2:p.Pro257Ala