Canonical Allele Identifier: CA2466504689

Gene: L1CAM

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153863531G= , CM000685.2:g.153863531G=	GRCh38
NC_000023.10:g.153128986G= , CM000685.1:g.153128986G=	GRCh37
NC_000023.9:g.152782180G=	NCBI36
NG_009645.3:g.50693C=
NG_009645.4:g.27643C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370060.7:c.3476C= MANE Select	ENSP00000359077.1:p.Thr1159=
ENST00000361699.8:c.3476C=	ENSP00000355380.4:p.Thr1159=
ENST00000361981.7:c.3461C=	ENSP00000354712.3:p.Thr1154=
ENST00000370055.5:c.3461C=	ENSP00000359072.1:p.Thr1154=
ENST00000370058.7:c.176C=	ENSP00000359075.3:p.Thr59=
ENST00000370060.5:c.3476C=	ENSP00000359077.1:p.Thr1159=
ENST00000491983.1:n.439C=
NM_000425.4:c.3476C=	NP_000416.1:p.Thr1159=
NM_001143963.2:c.3461C=	NP_001137435.1:p.Thr1154=
NM_001278116.1:c.3476C=	NP_001265045.1:p.Thr1159=
NM_024003.3:c.3476C=	NP_076493.1:p.Thr1159=
NM_000425.5:c.3476C=	NP_000416.1:p.Thr1159=
NM_001278116.2:c.3476C= MANE Select	NP_001265045.1:p.Thr1159=