Canonical Allele Identifier: CA2466507150
Gene: L1CAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153870409A= , CM000685.2:g.153870409A= GRCh38
NC_000023.10:g.153135864A= , CM000685.1:g.153135864A= GRCh37
NC_000023.9:g.152789058A= NCBI36
NG_009645.3:g.43815T=
NG_009645.4:g.20765T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370060.7:c.785T= MANE Select ENSP00000359077.1:p.Leu262=
ENST00000361699.8:c.785T= ENSP00000355380.4:p.Leu262=
ENST00000361981.7:c.770T= ENSP00000354712.3:p.Leu257=
ENST00000370055.5:c.770T= ENSP00000359072.1:p.Leu257=
ENST00000370060.5:c.785T= ENSP00000359077.1:p.Leu262=
NM_000425.4:c.785T= NP_000416.1:p.Leu262=
NM_001143963.2:c.770T= NP_001137435.1:p.Leu257=
NM_001278116.1:c.785T= NP_001265045.1:p.Leu262=
NM_024003.3:c.785T= NP_076493.1:p.Leu262=
NM_000425.5:c.785T= NP_000416.1:p.Leu262=
NM_001278116.2:c.785T= MANE Select NP_001265045.1:p.Leu262=