Canonical Allele Identifier: CA2466507116
Gene: L1CAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153870337G= , CM000685.2:g.153870337G= GRCh38
NC_000023.10:g.153135792G= , CM000685.1:g.153135792G= GRCh37
NC_000023.9:g.152788986G= NCBI36
NG_009645.3:g.43887C=
NG_009645.4:g.20837C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370060.7:c.806+51C= MANE Select ENSP00000359077.1:n.806+51C=
ENST00000361699.8:c.806+51C= ENSP00000355380.4:n.806+51C=
ENST00000361981.7:c.791+51C= ENSP00000354712.3:n.791+51C=
ENST00000370055.5:c.791+51C= ENSP00000359072.1:n.791+51C=
ENST00000370060.5:c.806+51C= ENSP00000359077.1:n.806+51C=
NM_000425.4:c.806+51C= NP_000416.1:n.806+51C=
NM_001143963.2:c.791+51C= NP_001137435.1:n.791+51C=
NM_001278116.1:c.806+51C= NP_001265045.1:n.806+51C=
NM_024003.3:c.806+51C= NP_076493.1:n.806+51C=
NM_000425.5:c.806+51C= NP_000416.1:n.806+51C=
NM_001278116.2:c.806+51C= MANE Select NP_001265045.1:n.806+51C=