Canonical Allele Identifier: CA2466506952

Gene: L1CAM

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153869905T= , CM000685.2:g.153869905T=	GRCh38
NC_000023.10:g.153135360T= , CM000685.1:g.153135360T=	GRCh37
NC_000023.9:g.152788554T=	NCBI36
NG_009645.3:g.44319A=
NG_009645.4:g.21269A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370060.7:c.1021A= MANE Select	ENSP00000359077.1:p.Ser341=
ENST00000361699.8:c.1021A=	ENSP00000355380.4:p.Ser341=
ENST00000361981.7:c.1006A=	ENSP00000354712.3:p.Ser336=
ENST00000370055.5:c.1006A=	ENSP00000359072.1:p.Ser336=
ENST00000370060.5:c.1021A=	ENSP00000359077.1:p.Ser341=
NM_000425.4:c.1021A=	NP_000416.1:p.Ser341=
NM_001143963.2:c.1006A=	NP_001137435.1:p.Ser336=
NM_001278116.1:c.1021A=	NP_001265045.1:p.Ser341=
NM_024003.3:c.1021A=	NP_076493.1:p.Ser341=
NM_000425.5:c.1021A=	NP_000416.1:p.Ser341=
NM_001278116.2:c.1021A= MANE Select	NP_001265045.1:p.Ser341=