Canonical Allele Identifier: CA10554048
Community Standard Title: NM_001278116.2(L1CAM):c.3000C>T (p.Gly1000=)
Gene: L1CAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153864867G>A , CM000685.2:g.153864867G>A GRCh38
NC_000023.10:g.153130322G>A , CM000685.1:g.153130322G>A GRCh37
NC_000023.9:g.152783516G>A NCBI36
NG_009645.3:g.49357C>T
NG_009645.4:g.26307C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001278116.2:c.3000C>T MANE Select NP_001265045.1:p.Gly1000=
ENST00000370060.7:c.3000C>T MANE Select ENSP00000359077.1:p.Gly1000=
NM_000425.4:c.3000C>T NP_000416.1:p.Gly1000=
NM_000425.5:c.3000C>T NP_000416.1:p.Gly1000=
NM_001143963.2:c.2985C>T NP_001137435.1:p.Gly995=
NM_001278116.1:c.3000C>T NP_001265045.1:p.Gly1000=
NM_024003.3:c.3000C>T NP_076493.1:p.Gly1000=
ENST00000361699.8:c.3000C>T ENSP00000355380.4:p.Gly1000=
ENST00000361981.7:c.2985C>T ENSP00000354712.3:p.Gly995=
ENST00000370055.5:c.2985C>T ENSP00000359072.1:p.Gly995=
ENST00000370060.5:c.3000C>T ENSP00000359077.1:p.Gly1000=