Canonical Allele Identifier: CA873291454

Gene: L1CAM

Linked Data

• dbSNP Id: rs1013750875
• gnomAD v3: X-153870590-C-G
• gnomAD v4: X-153870590-C-G
• MyVariant Identifiers: chrX:g.153870590C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153870590C>G , CM000685.2:g.153870590C>G	GRCh38
NC_000023.10:g.153136045C>G , CM000685.1:g.153136045C>G	GRCh37
NC_000023.9:g.152789239C>G	NCBI36
NG_009645.3:g.43634G>C
NG_009645.4:g.20584G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370060.7:c.695-91G>C MANE Select	ENSP00000359077.1:n.695-91G>C
ENST00000361699.8:c.695-91G>C	ENSP00000355380.4:n.695-91G>C
ENST00000361981.7:c.680-91G>C	ENSP00000354712.3:n.680-91G>C
ENST00000370055.5:c.680-91G>C	ENSP00000359072.1:n.680-91G>C
ENST00000370060.5:c.695-91G>C	ENSP00000359077.1:n.695-91G>C
NM_000425.4:c.695-91G>C	NP_000416.1:n.695-91G>C
NM_001143963.2:c.680-91G>C	NP_001137435.1:n.680-91G>C
NM_001278116.1:c.695-91G>C	NP_001265045.1:n.695-91G>C
NM_024003.3:c.695-91G>C	NP_076493.1:n.695-91G>C
NM_000425.5:c.695-91G>C	NP_000416.1:n.695-91G>C
NM_001278116.2:c.695-91G>C MANE Select	NP_001265045.1:n.695-91G>C