Canonical Allele Identifier: CA2454873113
Gene: LAMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.120448989_120448990delinsAT , CM000685.2:g.120448989_120448990delinsAT GRCh38
NC_000023.10:g.119582844_119582845delinsAT , CM000685.1:g.119582844_119582845delinsAT GRCh37
NC_000023.9:g.119466872_119466873delinsAT NCBI36
NG_007995.1:g.25360_25361delinsAT , LRG_749:g.25360_25361delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000706600.1:c.536_537delinsAT ENSP00000516464.1:p.Asn179=
ENST00000200639.9:c.536_537delinsAT MANE Select ENSP00000200639.4:p.Asn179=
ENST00000200639.8:c.536_537delinsAT ENSP00000200639.4:p.Asn179=
ENST00000371335.4:c.536_537delinsAT ENSP00000360386.4:p.Asn179=
ENST00000434600.6:c.536_537delinsAT ENSP00000408411.2:p.Asn179=
ENST00000486593.5:c.79_80delinsAT
NM_001122606.1:c.536_537delinsAT , LRG_749t3:c.536_537delinsAT NP_001116078.1:p.Asn179=
NM_002294.2:c.536_537delinsAT , LRG_749t1:c.536_537delinsAT NP_002285.1:p.Asn179=
NM_013995.2:c.536_537delinsAT , LRG_749t2:c.536_537delinsAT NP_054701.1:p.Asn179=
NM_002294.3:c.536_537delinsAT MANE Select NP_002285.1:p.Asn179=