Canonical Allele Identifier: CA2466506081
Gene: L1CAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153866831T= , CM000685.2:g.153866831T= GRCh38
NC_000023.10:g.153132286T= , CM000685.1:g.153132286T= GRCh37
NC_000023.9:g.152785480T= NCBI36
NG_009645.3:g.47393A=
NG_009645.4:g.24343A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370060.7:c.2249A= MANE Select ENSP00000359077.1:p.Tyr750=
ENST00000361699.8:c.2249A= ENSP00000355380.4:p.Tyr750=
ENST00000361981.7:c.2234A= ENSP00000354712.3:p.Tyr745=
ENST00000370055.5:c.2234A= ENSP00000359072.1:p.Tyr745=
ENST00000370060.5:c.2249A= ENSP00000359077.1:p.Tyr750=
ENST00000455590.1:c.511A=
NM_000425.4:c.2249A= NP_000416.1:p.Tyr750=
NM_001143963.2:c.2234A= NP_001137435.1:p.Tyr745=
NM_001278116.1:c.2249A= NP_001265045.1:p.Tyr750=
NM_024003.3:c.2249A= NP_076493.1:p.Tyr750=
NM_000425.5:c.2249A= NP_000416.1:p.Tyr750=
NM_001278116.2:c.2249A= MANE Select NP_001265045.1:p.Tyr750=