Canonical Allele Identifier: CA88719952

Gene: LAMP3

Linked Data

• dbSNP Id: rs1044751560
• gnomAD v4: 3-183152501-A-G
• MyVariant Identifiers: chr3:g.182870289A>G (hg19) ; chr3:g.183152501A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183152501A>G , CM000665.2:g.183152501A>G	GRCh38
NC_000003.11:g.182870289A>G , CM000665.1:g.182870289A>G	GRCh37
NC_000003.10:g.184352983A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265598.8:c.762T>C MANE Select	ENSP00000265598.3:p.Val254=
ENST00000265598.7:c.762T>C	ENSP00000265598.3:p.Val254=
ENST00000466939.1:c.690T>C	ENSP00000418912.1:p.Val230=
NM_014398.3:c.762T>C	NP_055213.2:p.Val254=
XM_005247360.3:c.762T>C	XP_005247417.1:p.Val254=
XM_006713586.2:c.690T>C	XP_006713649.1:p.Val230=
XM_011512688.1:c.762T>C	XP_011510990.1:p.Val254=
XR_924123.1:n.822T>C
XR_924124.1:n.822T>C
XM_005247360.5:c.762T>C	XP_005247417.1:p.Val254=
XM_006713586.3:c.690T>C	XP_006713649.1:p.Val230=
XM_011512688.2:c.762T>C	XP_011510990.1:p.Val254=
XM_024453453.1:c.690T>C	XP_024309221.1:p.Val230=
NM_014398.4:c.762T>C MANE Select	NP_055213.2:p.Val254=