Canonical Allele Identifier: CA10554254
Community Standard Title: NM_001278116.2(L1CAM):c.1974G>A (p.Ala658=)
Gene: L1CAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153867519C>T , CM000685.2:g.153867519C>T GRCh38
NC_000023.10:g.153132974C>T , CM000685.1:g.153132974C>T GRCh37
NC_000023.9:g.152786168C>T NCBI36
NG_009645.3:g.46705G>A
NG_009645.4:g.23655G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001278116.2:c.1974G>A MANE Select NP_001265045.1:p.Ala658=
ENST00000370060.7:c.1974G>A MANE Select ENSP00000359077.1:p.Ala658=
NM_000425.4:c.1974G>A NP_000416.1:p.Ala658=
NM_000425.5:c.1974G>A NP_000416.1:p.Ala658=
NM_001143963.2:c.1959G>A NP_001137435.1:p.Ala653=
NM_001278116.1:c.1974G>A NP_001265045.1:p.Ala658=
NM_024003.3:c.1974G>A NP_076493.1:p.Ala658=
ENST00000361699.8:c.1974G>A ENSP00000355380.4:p.Ala658=
ENST00000361981.7:c.1959G>A ENSP00000354712.3:p.Ala653=
ENST00000370055.5:c.1959G>A ENSP00000359072.1:p.Ala653=
ENST00000370060.5:c.1974G>A ENSP00000359077.1:p.Ala658=
ENST00000455590.1:c.236G>A