Canonical Allele Identifier: CA2466507364
Gene: L1CAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153871019_153871020delinsAC , CM000685.2:g.153871019_153871020delinsAC GRCh38
NC_000023.10:g.153136474_153136475delinsAC , CM000685.1:g.153136474_153136475delinsAC GRCh37
NC_000023.9:g.152789668_152789669delinsAC NCBI36
NG_009645.3:g.43204_43205delinsGT
NG_009645.4:g.20154_20155delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000370060.7:c.523+37_523+38delinsGT MANE Select ENSP00000359077.1:n.523+37_523+38delinsGT
ENST00000361699.8:c.523+37_523+38delinsGT ENSP00000355380.4:n.523+37_523+38delinsGT
ENST00000361981.7:c.508+37_508+38delinsGT ENSP00000354712.3:n.508+37_508+38delinsGT
ENST00000370055.5:c.508+37_508+38delinsGT ENSP00000359072.1:n.508+37_508+38delinsGT
ENST00000370060.5:c.523+37_523+38delinsGT ENSP00000359077.1:n.523+37_523+38delinsGT
NM_000425.4:c.523+37_523+38delinsGT NP_000416.1:n.523+37_523+38delinsGT
NM_001143963.2:c.508+37_508+38delinsGT NP_001137435.1:n.508+37_508+38delinsGT
NM_001278116.1:c.523+37_523+38delinsGT NP_001265045.1:n.523+37_523+38delinsGT
NM_024003.3:c.523+37_523+38delinsGT NP_076493.1:n.523+37_523+38delinsGT
NM_000425.5:c.523+37_523+38delinsGT NP_000416.1:n.523+37_523+38delinsGT
NM_001278116.2:c.523+37_523+38delinsGT MANE Select NP_001265045.1:n.523+37_523+38delinsGT