Canonical Allele Identifier: CA415133104

Gene: L1CAM

Linked Data

• MyVariant Identifiers: chrX:g.153135876T>A (hg19) ; chrX:g.153870421T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153870421T>A , CM000685.2:g.153870421T>A	GRCh38
NC_000023.10:g.153135876T>A , CM000685.1:g.153135876T>A	GRCh37
NC_000023.9:g.152789070T>A	NCBI36
NG_009645.3:g.43803A>T
NG_009645.4:g.20753A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370060.7:c.773A>T MANE Select	ENSP00000359077.1:p.Gln258Leu
ENST00000361699.8:c.773A>T	ENSP00000355380.4:p.Gln258Leu
ENST00000361981.7:c.758A>T	ENSP00000354712.3:p.Gln253Leu
ENST00000370055.5:c.758A>T	ENSP00000359072.1:p.Gln253Leu
ENST00000370060.5:c.773A>T	ENSP00000359077.1:p.Gln258Leu
NM_000425.4:c.773A>T	NP_000416.1:p.Gln258Leu
NM_001143963.2:c.758A>T	NP_001137435.1:p.Gln253Leu
NM_001278116.1:c.773A>T	NP_001265045.1:p.Gln258Leu
NM_024003.3:c.773A>T	NP_076493.1:p.Gln258Leu
NM_000425.5:c.773A>T	NP_000416.1:p.Gln258Leu
NM_001278116.2:c.773A>T MANE Select	NP_001265045.1:p.Gln258Leu