Canonical Allele Identifier: CA2697544837
Gene: L1CAM HGNC NCBI

Linked Data

ClinVar Variation Id: 2703967
ClinVar RCV Id: RCV003589782

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153870334_153870382delinsTCTTGATCTGTGTCGCCTTTTCCCTGGGGTTTTCCCTTCGCATTCCATCCTCCCTGAGCTTTCTGCTTCCTGAGCGCTCTCCT , CM000685.2:g.153870334_153870382delinsTCTTGATCTGTGTCGCCTTTTCCCTGGGGTTTTCCCTTCGCATTCCATCCTCCCTGAGCTTTCTGCTTCCTGAGCGCTCTCCT GRCh38
NC_000023.10:g.153135789_153135837delinsTCTTGATCTGTGTCGCCTTTTCCCTGGGGTTTTCCCTTCGCATTCCATCCTCCCTGAGCTTTCTGCTTCCTGAGCGCTCTCCT , CM000685.1:g.153135789_153135837delinsTCTTGATCTGTGTCGCCTTTTCCCTGGGGTTTTCCCTTCGCATTCCATCCTCCCTGAGCTTTCTGCTTCCTGAGCGCTCTCCT GRCh37
NC_000023.9:g.152788983_152789031delinsTCTTGATCTGTGTCGCCTTTTCCCTGGGGTTTTCCCTTCGCATTCCATCCTCCCTGAGCTTTCTGCTTCCTGAGCGCTCTCCT NCBI36
NG_009645.3:g.43842_43890delinsAGGAGAGCGCTCAGGAAGCAGAAAGCTCAGGGAGGATGGAATGCGAAGGGAAAACCCCAGGGAAAAGGCGACACAGATCAAGA
NG_009645.4:g.20792_20840delinsAGGAGAGCGCTCAGGAAGCAGAAAGCTCAGGGAGGATGGAATGCGAAGGGAAAACCCCAGGGAAAAGGCGACACAGATCAAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000370060.7:c.806+6_806+54delinsAGGAGAGCGCTCAGGAAGCAGAAAGCTCAGGGAGGATGGAATGCGAAGGGAAAACCCCAGGGAAAAGGCGACACAGATCAAGA MANE Select ENSP00000359077.1:n.806+6_806+54delinsAGGAGAGCGCTCAGGAAGCAGAA...
ENST00000361699.8:c.806+6_806+54delinsAGGAGAGCGCTCAGGAAGCAGAAAGCTCAGGGAGGATGGAATGCGAAGGGAAAACCCCAGGGAAAAGGCGACACAGATCAAGA ENSP00000355380.4:n.806+6_806+54delinsAGGAGAGCGCTCAGGAAGCAGAA...
ENST00000361981.7:c.791+6_791+54delinsAGGAGAGCGCTCAGGAAGCAGAAAGCTCAGGGAGGATGGAATGCGAAGGGAAAACCCCAGGGAAAAGGCGACACAGATCAAGA ENSP00000354712.3:n.791+6_791+54delinsAGGAGAGCGCTCAGGAAGCAGAA...
ENST00000370055.5:c.791+6_791+54delinsAGGAGAGCGCTCAGGAAGCAGAAAGCTCAGGGAGGATGGAATGCGAAGGGAAAACCCCAGGGAAAAGGCGACACAGATCAAGA ENSP00000359072.1:n.791+6_791+54delinsAGGAGAGCGCTCAGGAAGCAGAA...
ENST00000370060.5:c.806+6_806+54delinsAGGAGAGCGCTCAGGAAGCAGAAAGCTCAGGGAGGATGGAATGCGAAGGGAAAACCCCAGGGAAAAGGCGACACAGATCAAGA ENSP00000359077.1:n.806+6_806+54delinsAGGAGAGCGCTCAGGAAGCAGAA...
NM_000425.4:c.806+6_806+54delinsAGGAGAGCGCTCAGGAAGCAGAAAGCTCAGGGAGGATGGAATGCGAAGGGAAAACCCCAGGGAAAAGGCGACACAGATCAAGA NP_000416.1:n.806+6_806+54delinsAGGAGAGCGCTCAGGAAGCAGAAAGCTCA...
NM_001143963.2:c.791+6_791+54delinsAGGAGAGCGCTCAGGAAGCAGAAAGCTCAGGGAGGATGGAATGCGAAGGGAAAACCCCAGGGAAAAGGCGACACAGATCAAGA NP_001137435.1:n.791+6_791+54delinsAGGAGAGCGCTCAGGAAGCAGAAAGC...
NM_001278116.1:c.806+6_806+54delinsAGGAGAGCGCTCAGGAAGCAGAAAGCTCAGGGAGGATGGAATGCGAAGGGAAAACCCCAGGGAAAAGGCGACACAGATCAAGA NP_001265045.1:n.806+6_806+54delinsAGGAGAGCGCTCAGGAAGCAGAAAGC...
NM_024003.3:c.806+6_806+54delinsAGGAGAGCGCTCAGGAAGCAGAAAGCTCAGGGAGGATGGAATGCGAAGGGAAAACCCCAGGGAAAAGGCGACACAGATCAAGA NP_076493.1:n.806+6_806+54delinsAGGAGAGCGCTCAGGAAGCAGAAAGCTCA...
NM_000425.5:c.806+6_806+54delinsAGGAGAGCGCTCAGGAAGCAGAAAGCTCAGGGAGGATGGAATGCGAAGGGAAAACCCCAGGGAAAAGGCGACACAGATCAAGA NP_000416.1:n.806+6_806+54delinsAGGAGAGCGCTCAGGAAGCAGAAAGCTCA...
NM_001278116.2:c.806+6_806+54delinsAGGAGAGCGCTCAGGAAGCAGAAAGCTCAGGGAGGATGGAATGCGAAGGGAAAACCCCAGGGAAAAGGCGACACAGATCAAGA MANE Select NP_001265045.1:n.806+6_806+54delinsAGGAGAGCGCTCAGGAAGCAGAAAGC...