Canonical Allele Identifier: CA337261327
Community Standard Title: NM_001278116.2(L1CAM):c.2209-9C>T
Gene: L1CAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153866880G>A , CM000685.2:g.153866880G>A GRCh38
NC_000023.10:g.153132335G>A , CM000685.1:g.153132335G>A GRCh37
NC_000023.9:g.152785529G>A NCBI36
NG_009645.3:g.47344C>T
NG_009645.4:g.24294C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001278116.2:c.2209-9C>T MANE Select NP_001265045.1:n.2209-9C>T
ENST00000370060.7:c.2209-9C>T MANE Select ENSP00000359077.1:n.2209-9C>T
NM_000425.4:c.2209-9C>T NP_000416.1:n.2209-9C>T
NM_000425.5:c.2209-9C>T NP_000416.1:n.2209-9C>T
NM_001143963.2:c.2194-9C>T NP_001137435.1:n.2194-9C>T
NM_001278116.1:c.2209-9C>T NP_001265045.1:n.2209-9C>T
NM_024003.3:c.2209-9C>T NP_076493.1:n.2209-9C>T
ENST00000361699.8:c.2209-9C>T ENSP00000355380.4:n.2209-9C>T
ENST00000361981.7:c.2194-9C>T ENSP00000354712.3:n.2194-9C>T
ENST00000370055.5:c.2194-9C>T ENSP00000359072.1:n.2194-9C>T
ENST00000370060.5:c.2209-9C>T ENSP00000359077.1:n.2209-9C>T
ENST00000455590.1:c.471-9C>T