Canonical Allele Identifier: CA10602720
Community Standard Title: NM_001278116.2(L1CAM):c.1615T>G (p.Cys539Gly)
Gene: L1CAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153868390A>C , CM000685.2:g.153868390A>C GRCh38
NC_000023.10:g.153133845A>C , CM000685.1:g.153133845A>C GRCh37
NC_000023.9:g.152787039A>C NCBI36
NG_009645.3:g.45834T>G
NG_009645.4:g.22784T>G

Transcript Alleles

HGVS Amino-acid Change
NM_001278116.2:c.1615T>G MANE Select NP_001265045.1:p.Cys539Gly
ENST00000370060.7:c.1615T>G MANE Select ENSP00000359077.1:p.Cys539Gly
NM_000425.4:c.1615T>G NP_000416.1:p.Cys539Gly
NM_000425.5:c.1615T>G NP_000416.1:p.Cys539Gly
NM_001143963.2:c.1600T>G NP_001137435.1:p.Cys534Gly
NM_001278116.1:c.1615T>G NP_001265045.1:p.Cys539Gly
NM_024003.3:c.1615T>G NP_076493.1:p.Cys539Gly
ENST00000361699.8:c.1615T>G ENSP00000355380.4:p.Cys539Gly
ENST00000361981.7:c.1600T>G ENSP00000354712.3:p.Cys534Gly
ENST00000370055.5:c.1600T>G ENSP00000359072.1:p.Cys534Gly
ENST00000370060.5:c.1615T>G ENSP00000359077.1:p.Cys539Gly
ENST00000496122.1:n.234T>G