Canonical Allele Identifier: CA415133229

Gene: L1CAM

Linked Data

• MyVariant Identifiers: chrX:g.153135895G>T (hg19) ; chrX:g.153870440G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153870440G>T , CM000685.2:g.153870440G>T	GRCh38
NC_000023.10:g.153135895G>T , CM000685.1:g.153135895G>T	GRCh37
NC_000023.9:g.152789089G>T	NCBI36
NG_009645.3:g.43784C>A
NG_009645.4:g.20734C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370060.7:c.754C>A MANE Select	ENSP00000359077.1:p.Leu252Met
ENST00000361699.8:c.754C>A	ENSP00000355380.4:p.Leu252Met
ENST00000361981.7:c.739C>A	ENSP00000354712.3:p.Leu247Met
ENST00000370055.5:c.739C>A	ENSP00000359072.1:p.Leu247Met
ENST00000370060.5:c.754C>A	ENSP00000359077.1:p.Leu252Met
NM_000425.4:c.754C>A	NP_000416.1:p.Leu252Met
NM_001143963.2:c.739C>A	NP_001137435.1:p.Leu247Met
NM_001278116.1:c.754C>A	NP_001265045.1:p.Leu252Met
NM_024003.3:c.754C>A	NP_076493.1:p.Leu252Met
NM_000425.5:c.754C>A	NP_000416.1:p.Leu252Met
NM_001278116.2:c.754C>A MANE Select	NP_001265045.1:p.Leu252Met