Canonical Allele Identifier: CA2579733022
Gene: L1CAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153870548del , CM000685.2:g.153870548del GRCh38
NC_000023.10:g.153136003del , CM000685.1:g.153136003del GRCh37
NC_000023.9:g.152789197del NCBI36
NG_009645.3:g.43679del
NG_009645.4:g.20629del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370060.7:c.695-46del MANE Select ENSP00000359077.1:n.695-46del
ENST00000361699.8:c.695-46del ENSP00000355380.4:n.695-46del
ENST00000361981.7:c.680-46del ENSP00000354712.3:n.680-46del
ENST00000370055.5:c.680-46del ENSP00000359072.1:n.680-46del
ENST00000370060.5:c.695-46del ENSP00000359077.1:n.695-46del
NM_000425.4:c.695-46del NP_000416.1:n.695-46del
NM_001143963.2:c.680-46del NP_001137435.1:n.680-46del
NM_001278116.1:c.695-46del NP_001265045.1:n.695-46del
NM_024003.3:c.695-46del NP_076493.1:n.695-46del
NM_000425.5:c.695-46del NP_000416.1:n.695-46del
NM_001278116.2:c.695-46del MANE Select NP_001265045.1:n.695-46del