Canonical Allele Identifier: CA1425434390

Gene: LAMP3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183152729_183152730delinsCA , CM000665.2:g.183152729_183152730delinsCA	GRCh38
NC_000003.11:g.182870517_182870518delinsCA , CM000665.1:g.182870517_182870518delinsCA	GRCh37
NC_000003.10:g.184353211_184353212delinsCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265598.8:c.760-227_760-226delinsTG MANE Select	ENSP00000265598.3:n.760-227_760-226delinsTG
ENST00000265598.7:c.760-227_760-226delinsTG	ENSP00000265598.3:n.760-227_760-226delinsTG
ENST00000466939.1:c.688-227_688-226delinsTG	ENSP00000418912.1:n.688-227_688-226delinsTG
NM_014398.3:c.760-227_760-226delinsTG	NP_055213.2:n.760-227_760-226delinsTG
XM_005247360.3:c.760-227_760-226delinsTG	XP_005247417.1:n.760-227_760-226delinsTG
XM_006713586.2:c.688-227_688-226delinsTG	XP_006713649.1:n.688-227_688-226delinsTG
XM_011512688.1:c.760-227_760-226delinsTG	XP_011510990.1:n.760-227_760-226delinsTG
XR_924123.1:n.820-227_820-226delinsTG
XR_924124.1:n.820-227_820-226delinsTG
XM_005247360.5:c.760-227_760-226delinsTG	XP_005247417.1:n.760-227_760-226delinsTG
XM_006713586.3:c.688-227_688-226delinsTG	XP_006713649.1:n.688-227_688-226delinsTG
XM_011512688.2:c.760-227_760-226delinsTG	XP_011510990.1:n.760-227_760-226delinsTG
XM_024453453.1:c.688-227_688-226delinsTG	XP_024309221.1:n.688-227_688-226delinsTG
NM_014398.4:c.760-227_760-226delinsTG MANE Select	NP_055213.2:n.760-227_760-226delinsTG