Canonical Allele Identifier: CA2454871209
Gene: LAMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.120442669_120442670delinsGA , CM000685.2:g.120442669_120442670delinsGA GRCh38
NC_000023.10:g.119576524_119576525delinsGA , CM000685.1:g.119576524_119576525delinsGA GRCh37
NC_000023.9:g.119460552_119460553delinsGA NCBI36
NG_007995.1:g.31680_31681delinsTC , LRG_749:g.31680_31681delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000706600.1:c.865-8_865-7delinsTC ENSP00000516464.1:n.865-8_865-7delinsTC
ENST00000200639.9:c.865-8_865-7delinsTC MANE Select ENSP00000200639.4:n.865-8_865-7delinsTC
ENST00000200639.8:c.865-8_865-7delinsTC ENSP00000200639.4:n.865-8_865-7delinsTC
ENST00000371335.4:c.865-8_865-7delinsTC ENSP00000360386.4:n.865-8_865-7delinsTC
ENST00000434600.6:c.865-8_865-7delinsTC ENSP00000408411.2:n.865-8_865-7delinsTC
ENST00000486593.5:c.408-8_408-7delinsTC
NM_001122606.1:c.865-8_865-7delinsTC , LRG_749t3:c.865-8_865-7delinsTC NP_001116078.1:n.865-8_865-7delinsTC
NM_002294.2:c.865-8_865-7delinsTC , LRG_749t1:c.865-8_865-7delinsTC NP_002285.1:n.865-8_865-7delinsTC
NM_013995.2:c.865-8_865-7delinsTC , LRG_749t2:c.865-8_865-7delinsTC NP_054701.1:n.865-8_865-7delinsTC
NM_002294.3:c.865-8_865-7delinsTC MANE Select NP_002285.1:n.865-8_865-7delinsTC