Canonical Allele Identifier: CA2602676606

Gene: L1CAM

Linked Data

• dbSNP Id: rs2148498512
• gnomAD v3: X-153870621-A-C
• gnomAD v4: X-153870621-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153870621A>C , CM000685.2:g.153870621A>C	GRCh38
NC_000023.10:g.153136076A>C , CM000685.1:g.153136076A>C	GRCh37
NC_000023.9:g.152789270A>C	NCBI36
NG_009645.3:g.43603T>G
NG_009645.4:g.20553T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370060.7:c.695-122T>G MANE Select	ENSP00000359077.1:n.695-122T>G
ENST00000361699.8:c.695-122T>G	ENSP00000355380.4:n.695-122T>G
ENST00000361981.7:c.680-122T>G	ENSP00000354712.3:n.680-122T>G
ENST00000370055.5:c.680-122T>G	ENSP00000359072.1:n.680-122T>G
ENST00000370060.5:c.695-122T>G	ENSP00000359077.1:n.695-122T>G
NM_000425.4:c.695-122T>G	NP_000416.1:n.695-122T>G
NM_001143963.2:c.680-122T>G	NP_001137435.1:n.680-122T>G
NM_001278116.1:c.695-122T>G	NP_001265045.1:n.695-122T>G
NM_024003.3:c.695-122T>G	NP_076493.1:n.695-122T>G
NM_000425.5:c.695-122T>G	NP_000416.1:n.695-122T>G
NM_001278116.2:c.695-122T>G MANE Select	NP_001265045.1:n.695-122T>G