Canonical Allele Identifier: CA10554203
Community Standard Title: NM_001278116.2(L1CAM):c.2232C>T (p.Asn744=)
Gene: L1CAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153866848G>A , CM000685.2:g.153866848G>A GRCh38
NC_000023.10:g.153132303G>A , CM000685.1:g.153132303G>A GRCh37
NC_000023.9:g.152785497G>A NCBI36
NG_009645.3:g.47376C>T
NG_009645.4:g.24326C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001278116.2:c.2232C>T MANE Select NP_001265045.1:p.Asn744=
ENST00000370060.7:c.2232C>T MANE Select ENSP00000359077.1:p.Asn744=
NM_000425.4:c.2232C>T NP_000416.1:p.Asn744=
NM_000425.5:c.2232C>T NP_000416.1:p.Asn744=
NM_001143963.2:c.2217C>T NP_001137435.1:p.Asn739=
NM_001278116.1:c.2232C>T NP_001265045.1:p.Asn744=
NM_024003.3:c.2232C>T NP_076493.1:p.Asn744=
ENST00000361699.8:c.2232C>T ENSP00000355380.4:p.Asn744=
ENST00000361981.7:c.2217C>T ENSP00000354712.3:p.Asn739=
ENST00000370055.5:c.2217C>T ENSP00000359072.1:p.Asn739=
ENST00000370060.5:c.2232C>T ENSP00000359077.1:p.Asn744=
ENST00000455590.1:c.494C>T