Canonical Allele Identifier: CA437096283

Gene: LAMP3

Linked Data

• gnomAD v4: 3-183152447-C-G
• MyVariant Identifiers: chr3:g.182870235C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183152447C>G , CM000665.2:g.183152447C>G	GRCh38
NC_000003.11:g.182870235C>G , CM000665.1:g.182870235C>G	GRCh37
NC_000003.10:g.184352929C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265598.8:c.816G>C MANE Select	ENSP00000265598.3:p.Gly272=
ENST00000265598.7:c.816G>C	ENSP00000265598.3:p.Gly272=
ENST00000466939.1:c.744G>C	ENSP00000418912.1:p.Gly248=
NM_014398.3:c.816G>C	NP_055213.2:p.Gly272=
XM_005247360.3:c.816G>C	XP_005247417.1:p.Gly272=
XM_006713586.2:c.744G>C	XP_006713649.1:p.Gly248=
XM_011512688.1:c.816G>C	XP_011510990.1:p.Gly272=
XR_924123.1:n.876G>C
XR_924124.1:n.876G>C
XM_005247360.5:c.816G>C	XP_005247417.1:p.Gly272=
XM_006713586.3:c.744G>C	XP_006713649.1:p.Gly248=
XM_011512688.2:c.816G>C	XP_011510990.1:p.Gly272=
XM_024453453.1:c.744G>C	XP_024309221.1:p.Gly248=
NM_014398.4:c.816G>C MANE Select	NP_055213.2:p.Gly272=