Canonical Allele Identifier: CA2466507229

Gene: L1CAM

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153870620G= , CM000685.2:g.153870620G=	GRCh38
NC_000023.10:g.153136075G= , CM000685.1:g.153136075G=	GRCh37
NC_000023.9:g.152789269G=	NCBI36
NG_009645.3:g.43604C=
NG_009645.4:g.20554C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370060.7:c.695-121C= MANE Select	ENSP00000359077.1:n.695-121C=
ENST00000361699.8:c.695-121C=	ENSP00000355380.4:n.695-121C=
ENST00000361981.7:c.680-121C=	ENSP00000354712.3:n.680-121C=
ENST00000370055.5:c.680-121C=	ENSP00000359072.1:n.680-121C=
ENST00000370060.5:c.695-121C=	ENSP00000359077.1:n.695-121C=
NM_000425.4:c.695-121C=	NP_000416.1:n.695-121C=
NM_001143963.2:c.680-121C=	NP_001137435.1:n.680-121C=
NM_001278116.1:c.695-121C=	NP_001265045.1:n.695-121C=
NM_024003.3:c.695-121C=	NP_076493.1:n.695-121C=
NM_000425.5:c.695-121C=	NP_000416.1:n.695-121C=
NM_001278116.2:c.695-121C= MANE Select	NP_001265045.1:n.695-121C=