Canonical Allele Identifier: CA2466507218

Gene: L1CAM

Linked Data

• dbSNP Id: rs2064760187

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153870590_153870591dup , CM000685.2:g.153870590_153870591dup	GRCh38
NC_000023.10:g.153136045_153136046dup , CM000685.1:g.153136045_153136046dup	GRCh37
NC_000023.9:g.152789239_152789240dup	NCBI36
NG_009645.3:g.43633_43634dup
NG_009645.4:g.20583_20584dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370060.7:c.695-92_695-91dup MANE Select	ENSP00000359077.1:n.695-92_695-91dup
ENST00000361699.8:c.695-92_695-91dup	ENSP00000355380.4:n.695-92_695-91dup
ENST00000361981.7:c.680-92_680-91dup	ENSP00000354712.3:n.680-92_680-91dup
ENST00000370055.5:c.680-92_680-91dup	ENSP00000359072.1:n.680-92_680-91dup
ENST00000370060.5:c.695-92_695-91dup	ENSP00000359077.1:n.695-92_695-91dup
NM_000425.4:c.695-92_695-91dup	NP_000416.1:n.695-92_695-91dup
NM_001143963.2:c.680-92_680-91dup	NP_001137435.1:n.680-92_680-91dup
NM_001278116.1:c.695-92_695-91dup	NP_001265045.1:n.695-92_695-91dup
NM_024003.3:c.695-92_695-91dup	NP_076493.1:n.695-92_695-91dup
NM_000425.5:c.695-92_695-91dup	NP_000416.1:n.695-92_695-91dup
NM_001278116.2:c.695-92_695-91dup MANE Select	NP_001265045.1:n.695-92_695-91dup