Canonical Allele Identifier: CA1425434387

Gene: LAMP3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183152726_183152727delinsTG , CM000665.2:g.183152726_183152727delinsTG	GRCh38
NC_000003.11:g.182870514_182870515delinsTG , CM000665.1:g.182870514_182870515delinsTG	GRCh37
NC_000003.10:g.184353208_184353209delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265598.8:c.760-224_760-223delinsCA MANE Select	ENSP00000265598.3:n.760-224_760-223delinsCA
ENST00000265598.7:c.760-224_760-223delinsCA	ENSP00000265598.3:n.760-224_760-223delinsCA
ENST00000466939.1:c.688-224_688-223delinsCA	ENSP00000418912.1:n.688-224_688-223delinsCA
NM_014398.3:c.760-224_760-223delinsCA	NP_055213.2:n.760-224_760-223delinsCA
XM_005247360.3:c.760-224_760-223delinsCA	XP_005247417.1:n.760-224_760-223delinsCA
XM_006713586.2:c.688-224_688-223delinsCA	XP_006713649.1:n.688-224_688-223delinsCA
XM_011512688.1:c.760-224_760-223delinsCA	XP_011510990.1:n.760-224_760-223delinsCA
XR_924123.1:n.820-224_820-223delinsCA
XR_924124.1:n.820-224_820-223delinsCA
XM_005247360.5:c.760-224_760-223delinsCA	XP_005247417.1:n.760-224_760-223delinsCA
XM_006713586.3:c.688-224_688-223delinsCA	XP_006713649.1:n.688-224_688-223delinsCA
XM_011512688.2:c.760-224_760-223delinsCA	XP_011510990.1:n.760-224_760-223delinsCA
XM_024453453.1:c.688-224_688-223delinsCA	XP_024309221.1:n.688-224_688-223delinsCA
NM_014398.4:c.760-224_760-223delinsCA MANE Select	NP_055213.2:n.760-224_760-223delinsCA