Canonical Allele Identifier: CA1425434275

Gene: LAMP3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183152437_183152438delinsTG , CM000665.2:g.183152437_183152438delinsTG	GRCh38
NC_000003.11:g.182870225_182870226delinsTG , CM000665.1:g.182870225_182870226delinsTG	GRCh37
NC_000003.10:g.184352919_184352920delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265598.8:c.825_826delinsCA MANE Select	ENSP00000265598.3:p.Gly275=
ENST00000265598.7:c.825_826delinsCA	ENSP00000265598.3:p.Gly275=
ENST00000466939.1:c.753_754delinsCA	ENSP00000418912.1:p.Gly251=
NM_014398.3:c.825_826delinsCA	NP_055213.2:p.Gly275=
XM_005247360.3:c.825_826delinsCA	XP_005247417.1:p.Gly275=
XM_006713586.2:c.753_754delinsCA	XP_006713649.1:p.Gly251=
XM_011512688.1:c.825_826delinsCA	XP_011510990.1:p.Gly275=
XR_924123.1:n.885_886delinsCA
XR_924124.1:n.885_886delinsCA
XM_005247360.5:c.825_826delinsCA	XP_005247417.1:p.Gly275=
XM_006713586.3:c.753_754delinsCA	XP_006713649.1:p.Gly251=
XM_011512688.2:c.825_826delinsCA	XP_011510990.1:p.Gly275=
XM_024453453.1:c.753_754delinsCA	XP_024309221.1:p.Gly251=
NM_014398.4:c.825_826delinsCA MANE Select	NP_055213.2:p.Gly275=