Canonical Allele Identifier: CA415128786
Community Standard Title: NM_001278116.2(L1CAM):c.1268-1G>A
Gene: L1CAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153868953C>T , CM000685.2:g.153868953C>T GRCh38
NC_000023.9:g.152787602C>T NCBI36
NG_009645.3:g.45271G>A
NG_009645.4:g.22221G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001278116.2:c.1268-1G>A MANE Select NP_001265045.1:n.1268-1G>A
ENST00000370060.7:c.1268-1G>A MANE Select ENSP00000359077.1:n.1268-1G>A
NM_000425.4:c.1268-1G>A NP_000416.1:n.1268-1G>A
NM_000425.5:c.1268-1G>A NP_000416.1:n.1268-1G>A
NM_001143963.2:c.1253-1G>A NP_001137435.1:n.1253-1G>A
NM_001278116.1:c.1268-1G>A NP_001265045.1:n.1268-1G>A
NM_024003.3:c.1268-1G>A NP_076493.1:n.1268-1G>A
ENST00000361699.8:c.1268-1G>A ENSP00000355380.4:n.1268-1G>A
ENST00000361981.7:c.1253-1G>A ENSP00000354712.3:n.1253-1G>A
ENST00000370055.5:c.1253-1G>A ENSP00000359072.1:n.1253-1G>A
ENST00000370060.5:c.1268-1G>A ENSP00000359077.1:n.1268-1G>A
ENST00000484652.1:n.220G>A