Canonical Allele Identifier: CA437096308

Gene: LAMP3

Linked Data

• gnomAD v4: 3-183152477-G-A
• MyVariant Identifiers: chr3:g.182870265G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183152477G>A , CM000665.2:g.183152477G>A	GRCh38
NC_000003.11:g.182870265G>A , CM000665.1:g.182870265G>A	GRCh37
NC_000003.10:g.184352959G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265598.8:c.786C>T MANE Select	ENSP00000265598.3:p.Asn262=
ENST00000265598.7:c.786C>T	ENSP00000265598.3:p.Asn262=
ENST00000466939.1:c.714C>T	ENSP00000418912.1:p.Asn238=
NM_014398.3:c.786C>T	NP_055213.2:p.Asn262=
XM_005247360.3:c.786C>T	XP_005247417.1:p.Asn262=
XM_006713586.2:c.714C>T	XP_006713649.1:p.Asn238=
XM_011512688.1:c.786C>T	XP_011510990.1:p.Asn262=
XR_924123.1:n.846C>T
XR_924124.1:n.846C>T
XM_005247360.5:c.786C>T	XP_005247417.1:p.Asn262=
XM_006713586.3:c.714C>T	XP_006713649.1:p.Asn238=
XM_011512688.2:c.786C>T	XP_011510990.1:p.Asn262=
XM_024453453.1:c.714C>T	XP_024309221.1:p.Asn238=
NM_014398.4:c.786C>T MANE Select	NP_055213.2:p.Asn262=