Canonical Allele Identifier: CA174901
Gene: RLIM HGNC NCBI

Linked Data

ClinVar Variation Id: 161848
ClinVar RCV Id: RCV000149384
dbSNP Id: rs193920920
COSMIC: COSM1180178
MyVariant Identifiers: chrX:g.73812890del (hg19) chrX:g.74593055del (hg38)
PubMed: PMID:23265383
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74593055del , CM000685.2:g.74593055del GRCh38
NC_000023.10:g.73812890del , CM000685.1:g.73812890del GRCh37
NC_000023.9:g.73729615del NCBI36
NG_013258.1:g.26572del

Transcript Alleles

HGVS Amino-acid change
ENST00000332687.11:c.260del MANE Select ENSP00000328059.6:p.Asp87AlafsTer12
ENST00000332687.10:c.260del ENSP00000328059.6:p.Asp87AlafsTer12
ENST00000349225.2:c.260del ENSP00000253571.3:p.Asp87AlafsTer12
NM_016120.3:c.260del NP_057204.2:p.Asp87AlafsTer12
NM_183353.2:c.260del NP_899196.1:p.Asp87AlafsTer12
NM_016120.4:c.260del MANE Select NP_057204.2:p.Asp87AlafsTer12
NM_183353.3:c.260del NP_899196.1:p.Asp87AlafsTer12
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