Canonical Allele Identifier: CA415108477

Gene: L1CAM

Linked Data

• MyVariant Identifiers: chrX:g.153128949C>A (hg19) ; chrX:g.153863494C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153863494C>A , CM000685.2:g.153863494C>A	GRCh38
NC_000023.10:g.153128949C>A , CM000685.1:g.153128949C>A	GRCh37
NC_000023.9:g.152782143C>A	NCBI36
NG_009645.3:g.50730G>T
NG_009645.4:g.27680G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370060.7:c.3513G>T MANE Select	ENSP00000359077.1:p.Glu1171Asp
ENST00000361699.8:c.3513G>T	ENSP00000355380.4:p.Glu1171Asp
ENST00000361981.7:c.3498G>T	ENSP00000354712.3:p.Glu1166Asp
ENST00000370055.5:c.3498G>T	ENSP00000359072.1:p.Glu1166Asp
ENST00000370058.7:c.213G>T	ENSP00000359075.3:p.Glu71Asp
ENST00000370060.5:c.3513G>T	ENSP00000359077.1:p.Glu1171Asp
ENST00000491983.1:n.476G>T
NM_000425.4:c.3513G>T	NP_000416.1:p.Glu1171Asp
NM_001143963.2:c.3498G>T	NP_001137435.1:p.Glu1166Asp
NM_001278116.1:c.3513G>T	NP_001265045.1:p.Glu1171Asp
NM_024003.3:c.3513G>T	NP_076493.1:p.Glu1171Asp
NM_000425.5:c.3513G>T	NP_000416.1:p.Glu1171Asp
NM_001278116.2:c.3513G>T MANE Select	NP_001265045.1:p.Glu1171Asp