Canonical Allele Identifier: CA415120011
Community Standard Title: NM_001278116.2(L1CAM):c.2376C>G (p.Asn792Lys)
Gene: L1CAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153866704G>C , CM000685.2:g.153866704G>C GRCh38
NC_000023.10:g.153132159G>C , CM000685.1:g.153132159G>C GRCh37
NC_000023.9:g.152785353G>C NCBI36
NG_009645.3:g.47520C>G
NG_009645.4:g.24470C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001278116.2:c.2376C>G MANE Select NP_001265045.1:p.Asn792Lys
ENST00000370060.7:c.2376C>G MANE Select ENSP00000359077.1:p.Asn792Lys
NM_000425.4:c.2376C>G NP_000416.1:p.Asn792Lys
NM_000425.5:c.2376C>G NP_000416.1:p.Asn792Lys
NM_001143963.2:c.2361C>G NP_001137435.1:p.Asn787Lys
NM_001278116.1:c.2376C>G NP_001265045.1:p.Asn792Lys
NM_024003.3:c.2376C>G NP_076493.1:p.Asn792Lys
ENST00000361699.8:c.2376C>G ENSP00000355380.4:p.Asn792Lys
ENST00000361981.7:c.2361C>G ENSP00000354712.3:p.Asn787Lys
ENST00000370055.5:c.2361C>G ENSP00000359072.1:p.Asn787Lys
ENST00000370060.5:c.2376C>G ENSP00000359077.1:p.Asn792Lys