Canonical Allele Identifier: CA412793115
Gene: RBM10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47173126A>T , CM000685.2:g.47173126A>T GRCh38
NC_000023.10:g.47032525A>T , CM000685.1:g.47032525A>T GRCh37
NC_000023.9:g.46917469A>T NCBI36
NG_012548.1:g.32895A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000377604.8:c.433-2A>T MANE Select ENSP00000366829.3:n.433-2A>T
ENST00000329236.8:c.628-2A>T ENSP00000328848.8:n.628-2A>T
ENST00000345781.10:c.202-2A>T ENSP00000329659.6:n.202-2A>T
ENST00000377604.7:c.433-2A>T ENSP00000366829.3:n.433-2A>T
ENST00000628161.2:c.202-2A>T ENSP00000486115.1:n.202-2A>T
NM_001204466.1:c.202-2A>T NP_001191395.1:n.202-2A>T
NM_001204467.1:c.433-2A>T NP_001191396.1:n.433-2A>T
NM_001204468.1:c.628-2A>T NP_001191397.1:n.628-2A>T
NM_005676.4:c.433-2A>T NP_005667.2:n.433-2A>T
NM_152856.2:c.202-2A>T NP_690595.1:n.202-2A>T
XM_005272677.3:c.628-2A>T XP_005272734.1:n.628-2A>T
XM_005272678.3:c.397-2A>T XP_005272735.1:n.397-2A>T
XM_005272679.3:c.397-2A>T XP_005272736.1:n.397-2A>T
XM_006724563.1:c.-103-2A>T XP_006724626.1:n.-103-2A>T
XM_005272677.4:c.628-2A>T XP_005272734.1:n.628-2A>T
XM_005272678.4:c.397-2A>T XP_005272735.1:n.397-2A>T
XM_005272679.4:c.397-2A>T XP_005272736.1:n.397-2A>T
XM_017029884.2:c.-103-2A>T XP_016885373.1:n.-103-2A>T
XM_017029885.1:c.-103-2A>T XP_016885374.1:n.-103-2A>T
XM_024452457.1:c.628-2A>T XP_024308225.1:n.628-2A>T
XM_024452458.1:c.628-2A>T XP_024308226.1:n.628-2A>T
XM_024452459.1:c.433-2A>T XP_024308227.1:n.433-2A>T
XM_024452460.1:c.433-2A>T XP_024308228.1:n.433-2A>T
XM_024452461.1:c.397-2A>T XP_024308229.1:n.397-2A>T
XM_024452462.1:c.202-2A>T XP_024308230.1:n.202-2A>T
XM_024452463.1:c.-103-2A>T XP_024308231.1:n.-103-2A>T
XM_024452464.1:c.-103-2A>T XP_024308232.1:n.-103-2A>T
NM_005676.5:c.433-2A>T MANE Select NP_005667.2:n.433-2A>T
NM_001204466.2:c.202-2A>T NP_001191395.1:n.202-2A>T
NM_001204467.2:c.433-2A>T NP_001191396.1:n.433-2A>T
NM_152856.3:c.202-2A>T NP_690595.1:n.202-2A>T
NM_001204468.2:c.628-2A>T NP_001191397.1:n.628-2A>T