Canonical Allele Identifier: CA2466507155
Gene: L1CAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153870422G= , CM000685.2:g.153870422G= GRCh38
NC_000023.10:g.153135877G= , CM000685.1:g.153135877G= GRCh37
NC_000023.9:g.152789071G= NCBI36
NG_009645.3:g.43802C=
NG_009645.4:g.20752C=

Transcript Alleles

HGVS Amino-acid change
ENST00000370060.7:c.772C= MANE Select ENSP00000359077.1:p.Gln258=
ENST00000361699.8:c.772C= ENSP00000355380.4:p.Gln258=
ENST00000361981.7:c.757C= ENSP00000354712.3:p.Gln253=
ENST00000370055.5:c.757C= ENSP00000359072.1:p.Gln253=
ENST00000370060.5:c.772C= ENSP00000359077.1:p.Gln258=
NM_000425.4:c.772C= NP_000416.1:p.Gln258=
NM_001143963.2:c.757C= NP_001137435.1:p.Gln253=
NM_001278116.1:c.772C= NP_001265045.1:p.Gln258=
NM_024003.3:c.772C= NP_076493.1:p.Gln258=
NM_000425.5:c.772C= NP_000416.1:p.Gln258=
NM_001278116.2:c.772C= MANE Select NP_001265045.1:p.Gln258=