Canonical Allele Identifier: CA2466504816

Gene: L1CAM

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153863818G= , CM000685.2:g.153863818G=	GRCh38
NC_000023.10:g.153129273G= , CM000685.1:g.153129273G=	GRCh37
NC_000023.9:g.152782467G=	NCBI36
NG_009645.3:g.50406C=
NG_009645.4:g.27356C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370060.7:c.3457+65C= MANE Select	ENSP00000359077.1:n.3457+65C=
ENST00000361699.8:c.3457+65C=	ENSP00000355380.4:n.3457+65C=
ENST00000361981.7:c.3442+65C=	ENSP00000354712.3:n.3442+65C=
ENST00000370055.5:c.3442+65C=	ENSP00000359072.1:n.3442+65C=
ENST00000370058.7:c.158-269C=	ENSP00000359075.3:n.158-269C=
ENST00000370060.5:c.3457+65C=	ENSP00000359077.1:n.3457+65C=
ENST00000491983.1:n.152C=
NM_000425.4:c.3457+65C=	NP_000416.1:n.3457+65C=
NM_001143963.2:c.3442+65C=	NP_001137435.1:n.3442+65C=
NM_001278116.1:c.3457+65C=	NP_001265045.1:n.3457+65C=
NM_024003.3:c.3457+65C=	NP_076493.1:n.3457+65C=
NM_000425.5:c.3457+65C=	NP_000416.1:n.3457+65C=
NM_001278116.2:c.3457+65C= MANE Select	NP_001265045.1:n.3457+65C=