Canonical Allele Identifier: CA1139667508

Gene: RBM10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47169414_47169429del , CM000685.2:g.47169414_47169429del	GRCh38
NC_000023.10:g.47028813_47028828del , CM000685.1:g.47028813_47028828del	GRCh37
NC_000023.9:g.46913757_46913772del	NCBI36
NG_012548.1:g.29183_29198del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377604.8:c.117_132del MANE Select	ENSP00000366829.3:p.Met39IlefsTer?
ENST00000329236.8:c.312_327del	ENSP00000328848.8:p.Met104IlefsTer?
ENST00000345781.10:c.117_132del	ENSP00000329659.6:p.Met39IlefsTer?
ENST00000377604.7:c.117_132del	ENSP00000366829.3:p.Met39IlefsTer?
ENST00000628161.2:c.117_132del	ENSP00000486115.1:p.Met39IlefsTer?
NM_001204466.1:c.117_132del	NP_001191395.1:p.Met39IlefsTer?
NM_001204467.1:c.117_132del	NP_001191396.1:p.Met39IlefsTer?
NM_001204468.1:c.312_327del	NP_001191397.1:p.Met104IlefsTer?
NM_005676.4:c.117_132del	NP_005667.2:p.Met39IlefsTer?
NM_152856.2:c.117_132del	NP_690595.1:p.Met39IlefsTer?
XM_005272677.3:c.312_327del	XP_005272734.1:p.Met104IlefsTer?
XM_005272678.3:c.312_327del	XP_005272735.1:p.Met104IlefsTer?
XM_005272679.3:c.312_327del	XP_005272736.1:p.Met104IlefsTer?
XM_006724563.1:c.-188_-173del	XP_006724626.1:n.-188_-173del
XM_005272677.4:c.312_327del	XP_005272734.1:p.Met104IlefsTer?
XM_005272678.4:c.312_327del	XP_005272735.1:p.Met104IlefsTer?
XM_005272679.4:c.312_327del	XP_005272736.1:p.Met104IlefsTer?
XM_017029884.2:c.-419_-404del	XP_016885373.1:n.-419_-404del
XM_017029885.1:c.-419_-404del	XP_016885374.1:n.-419_-404del
XM_024452457.1:c.312_327del	XP_024308225.1:p.Met104IlefsTer?
XM_024452458.1:c.312_327del	XP_024308226.1:p.Met104IlefsTer?
XM_024452459.1:c.117_132del	XP_024308227.1:p.Met39IlefsTer?
XM_024452460.1:c.117_132del	XP_024308228.1:p.Met39IlefsTer?
XM_024452461.1:c.312_327del	XP_024308229.1:p.Met104IlefsTer?
XM_024452462.1:c.117_132del	XP_024308230.1:p.Met39IlefsTer?
XM_024452463.1:c.-419_-404del	XP_024308231.1:n.-419_-404del
XM_024452464.1:c.-188_-173del	XP_024308232.1:n.-188_-173del
NM_005676.5:c.117_132del MANE Select	NP_005667.2:p.Met39IlefsTer?
NM_001204466.2:c.117_132del	NP_001191395.1:p.Met39IlefsTer?
NM_001204467.2:c.117_132del	NP_001191396.1:p.Met39IlefsTer?
NM_152856.3:c.117_132del	NP_690595.1:p.Met39IlefsTer?
NM_001204468.2:c.312_327del	NP_001191397.1:p.Met104IlefsTer?