Canonical Allele Identifier: CA16621410
Gene: RBM10 HGNC NCBI

Linked Data

ClinVar Variation Id: 421365
ClinVar RCV Id: RCV000479448
dbSNP Id: rs1064795088
MyVariant Identifiers: chrX:g.47040804del (hg19) chrX:g.47181405del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47181405del , CM000685.2:g.47181405del GRCh38
NC_000023.10:g.47040804del , CM000685.1:g.47040804del GRCh37
NC_000023.9:g.46925748del NCBI36
NG_012548.1:g.41174del

Transcript Alleles

HGVS Amino-acid change
ENST00000377604.8:c.1435+4del MANE Select ENSP00000366829.3:n.1435+4del
ENST00000329236.8:c.1630+4del ENSP00000328848.8:n.1630+4del
ENST00000345781.10:c.1204+4del ENSP00000329659.6:n.1204+4del
ENST00000377604.7:c.1435+4del ENSP00000366829.3:n.1435+4del
ENST00000478410.1:n.810+4del
ENST00000496012.6:n.355+4del
ENST00000628161.2:c.1201+4del ENSP00000486115.1:n.1201+4del
NM_001204466.1:c.1204+4del NP_001191395.1:n.1204+4del
NM_001204467.1:c.1432+4del NP_001191396.1:n.1432+4del
NM_001204468.1:c.1630+4del NP_001191397.1:n.1630+4del
NM_005676.4:c.1435+4del NP_005667.2:n.1435+4del
NM_152856.2:c.1201+4del NP_690595.1:n.1201+4del
XM_005272677.3:c.1627+4del XP_005272734.1:n.1627+4del
XM_005272678.3:c.1399+4del XP_005272735.1:n.1399+4del
XM_005272679.3:c.1396+4del XP_005272736.1:n.1396+4del
XM_006724563.1:c.826+4del XP_006724626.1:n.826+4del
XM_011543989.1:c.499+4del XP_011542291.1:n.499+4del
XM_005272677.4:c.1627+4del XP_005272734.1:n.1627+4del
XM_005272678.4:c.1399+4del XP_005272735.1:n.1399+4del
XM_005272679.4:c.1396+4del XP_005272736.1:n.1396+4del
XM_017029884.2:c.826+4del XP_016885373.1:n.826+4del
XM_017029885.1:c.823+4del XP_016885374.1:n.823+4del
XM_024452457.1:c.1630+4del XP_024308225.1:n.1630+4del
XM_024452458.1:c.1627+4del XP_024308226.1:n.1627+4del
XM_024452459.1:c.1435+4del XP_024308227.1:n.1435+4del
XM_024452460.1:c.1432+4del XP_024308228.1:n.1432+4del
XM_024452461.1:c.1399+4del XP_024308229.1:n.1399+4del
XM_024452462.1:c.1204+4del XP_024308230.1:n.1204+4del
XM_024452463.1:c.826+4del XP_024308231.1:n.826+4del
XM_024452464.1:c.826+4del XP_024308232.1:n.826+4del
XM_024452465.1:c.499+4del XP_024308233.1:n.499+4del
NM_005676.5:c.1435+4del MANE Select NP_005667.2:n.1435+4del
NM_001204466.2:c.1204+4del NP_001191395.1:n.1204+4del
NM_001204467.2:c.1432+4del NP_001191396.1:n.1432+4del
NM_152856.3:c.1201+4del NP_690595.1:n.1201+4del
NM_001204468.2:c.1630+4del NP_001191397.1:n.1630+4del
Search 100 bp 5'
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