Canonical Allele Identifier: CA2466504653
Gene: L1CAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153863423A= , CM000685.2:g.153863423A= GRCh38
NC_000023.10:g.153128878A= , CM000685.1:g.153128878A= GRCh37
NC_000023.9:g.152782072A= NCBI36
NG_009645.3:g.50801T=
NG_009645.4:g.27751T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370060.7:c.3531-44T= MANE Select ENSP00000359077.1:n.3531-44T=
ENST00000361699.8:c.3530+54T= ENSP00000355380.4:n.3530+54T=
ENST00000361981.7:c.3515+54T= ENSP00000354712.3:n.3515+54T=
ENST00000370055.5:c.3515+54T= ENSP00000359072.1:n.3515+54T=
ENST00000370058.7:c.230+54T= ENSP00000359075.3:n.230+54T=
ENST00000370060.5:c.3531-44T= ENSP00000359077.1:n.3531-44T=
ENST00000491983.1:n.494-44T=
NM_000425.4:c.3531-44T= NP_000416.1:n.3531-44T=
NM_001143963.2:c.3515+54T= NP_001137435.1:n.3515+54T=
NM_001278116.1:c.3531-44T= NP_001265045.1:n.3531-44T=
NM_024003.3:c.3530+54T= NP_076493.1:n.3530+54T=
NM_000425.5:c.3531-44T= NP_000416.1:n.3531-44T=
NM_001278116.2:c.3531-44T= MANE Select NP_001265045.1:n.3531-44T=