Canonical Allele Identifier: CA2466507149
Gene: L1CAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153870403C= , CM000685.2:g.153870403C= GRCh38
NC_000023.10:g.153135858C= , CM000685.1:g.153135858C= GRCh37
NC_000023.9:g.152789052C= NCBI36
NG_009645.3:g.43821G=
NG_009645.4:g.20771G=

Transcript Alleles

HGVS Amino-acid change
ENST00000370060.7:c.791G= MANE Select ENSP00000359077.1:p.Cys264=
ENST00000361699.8:c.791G= ENSP00000355380.4:p.Cys264=
ENST00000361981.7:c.776G= ENSP00000354712.3:p.Cys259=
ENST00000370055.5:c.776G= ENSP00000359072.1:p.Cys259=
ENST00000370060.5:c.791G= ENSP00000359077.1:p.Cys264=
NM_000425.4:c.791G= NP_000416.1:p.Cys264=
NM_001143963.2:c.776G= NP_001137435.1:p.Cys259=
NM_001278116.1:c.791G= NP_001265045.1:p.Cys264=
NM_024003.3:c.791G= NP_076493.1:p.Cys264=
NM_000425.5:c.791G= NP_000416.1:p.Cys264=
NM_001278116.2:c.791G= MANE Select NP_001265045.1:p.Cys264=