Canonical Allele Identifier: CA415130400
Gene: L1CAM HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.153135273C>G (hg19) chrX:g.153869818C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153869818C>G , CM000685.2:g.153869818C>G GRCh38
NC_000023.10:g.153135273C>G , CM000685.1:g.153135273C>G GRCh37
NC_000023.9:g.152788467C>G NCBI36
NG_009645.3:g.44406G>C
NG_009645.4:g.21356G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000370060.7:c.1108G>C MANE Select ENSP00000359077.1:p.Gly370Arg
ENST00000361699.8:c.1108G>C ENSP00000355380.4:p.Gly370Arg
ENST00000361981.7:c.1093G>C ENSP00000354712.3:p.Gly365Arg
ENST00000370055.5:c.1093G>C ENSP00000359072.1:p.Gly365Arg
ENST00000370060.5:c.1108G>C ENSP00000359077.1:p.Gly370Arg
NM_000425.4:c.1108G>C NP_000416.1:p.Gly370Arg
NM_001143963.2:c.1093G>C NP_001137435.1:p.Gly365Arg
NM_001278116.1:c.1108G>C NP_001265045.1:p.Gly370Arg
NM_024003.3:c.1108G>C NP_076493.1:p.Gly370Arg
NM_000425.5:c.1108G>C NP_000416.1:p.Gly370Arg
NM_001278116.2:c.1108G>C MANE Select NP_001265045.1:p.Gly370Arg
Search 100 bp 5'
Search 100 bp 3'