Canonical Allele Identifier: CA134078

Gene: LAMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.120456651A>T , CM000685.2:g.120456651A>T	GRCh38
NC_000023.10:g.119590506A>T , CM000685.1:g.119590506A>T	GRCh37
NC_000023.9:g.119474534A>T	NCBI36
NG_007995.1:g.17699T>A , LRG_749:g.17699T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002294.3:c.183T>A MANE Select	NP_002285.1:p.Tyr61Ter
ENST00000200639.9:c.183T>A MANE Select	ENSP00000200639.4:p.Tyr61Ter
NM_001122606.1:c.183T>A , LRG_749t3:c.183T>A	NP_001116078.1:p.Tyr61Ter
NM_002294.2:c.183T>A , LRG_749t1:c.183T>A	NP_002285.1:p.Tyr61Ter
NM_013995.2:c.183T>A , LRG_749t2:c.183T>A	NP_054701.1:p.Tyr61Ter
ENST00000200639.8:c.183T>A	ENSP00000200639.4:p.Tyr61Ter
ENST00000371335.4:c.183T>A	ENSP00000360386.4:p.Tyr61Ter
ENST00000434600.6:c.183T>A	ENSP00000408411.2:p.Tyr61Ter
ENST00000706600.1:c.183T>A	ENSP00000516464.1:p.Tyr61Ter