Canonical Allele Identifier: CA2579692179
Gene: LAMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.120448063G>A , CM000685.2:g.120448063G>A GRCh38
NC_000023.10:g.119581918G>A , CM000685.1:g.119581918G>A GRCh37
NC_000023.9:g.119465946G>A NCBI36
NG_007995.1:g.26287C>T , LRG_749:g.26287C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706600.1:c.557-38C>T ENSP00000516464.1:n.557-38C>T
ENST00000200639.9:c.557-38C>T MANE Select ENSP00000200639.4:n.557-38C>T
ENST00000200639.8:c.557-38C>T ENSP00000200639.4:n.557-38C>T
ENST00000371335.4:c.557-38C>T ENSP00000360386.4:n.557-38C>T
ENST00000434600.6:c.557-38C>T ENSP00000408411.2:n.557-38C>T
ENST00000486593.5:c.100-38C>T
NM_001122606.1:c.557-38C>T , LRG_749t3:c.557-38C>T NP_001116078.1:n.557-38C>T
NM_002294.2:c.557-38C>T , LRG_749t1:c.557-38C>T NP_002285.1:n.557-38C>T
NM_013995.2:c.557-38C>T , LRG_749t2:c.557-38C>T NP_054701.1:n.557-38C>T
NM_002294.3:c.557-38C>T MANE Select NP_002285.1:n.557-38C>T