Canonical Allele Identifier: CA2579732979
Gene: L1CAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153870206del , CM000685.2:g.153870206del GRCh38
NC_000023.10:g.153135661del , CM000685.1:g.153135661del GRCh37
NC_000023.9:g.152788855del NCBI36
NG_009645.3:g.44019del
NG_009645.4:g.20969del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370060.7:c.842del MANE Select ENSP00000359077.1:p.Gly281AlafsTer20
ENST00000361699.8:c.842del ENSP00000355380.4:p.Gly281AlafsTer20
ENST00000361981.7:c.827del ENSP00000354712.3:p.Gly276AlafsTer20
ENST00000370055.5:c.827del ENSP00000359072.1:p.Gly276AlafsTer20
ENST00000370060.5:c.842del ENSP00000359077.1:p.Gly281AlafsTer20
NM_000425.4:c.842del NP_000416.1:p.Gly281AlafsTer20
NM_001143963.2:c.827del NP_001137435.1:p.Gly276AlafsTer20
NM_001278116.1:c.842del NP_001265045.1:p.Gly281AlafsTer20
NM_024003.3:c.842del NP_076493.1:p.Gly281AlafsTer20
NM_000425.5:c.842del NP_000416.1:p.Gly281AlafsTer20
NM_001278116.2:c.842del MANE Select NP_001265045.1:p.Gly281AlafsTer20