Canonical Allele Identifier: CA2684771343
Gene: RBM28 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128330811_128330813del , CM000669.2:g.128330811_128330813del GRCh38
NC_000007.13:g.127970864_127970866del , CM000669.1:g.127970864_127970866del GRCh37
NC_000007.12:g.127758100_127758102del NCBI36
NG_015802.1:g.18100_18102del

Transcript Alleles

HGVS Amino-acid change
ENST00000223073.6:c.1129+9_1129+11del MANE Select ENSP00000223073.1:n.1129+9_1129+11del
ENST00000415472.6:c.706+9_706+11del ENSP00000390517.2:n.706+9_706+11del
ENST00000487602.5:c.546+9_546+11del
NM_001166135.1:c.706+9_706+11del NP_001159607.1:n.706+9_706+11del
NM_018077.2:c.1129+9_1129+11del NP_060547.2:n.1129+9_1129+11del
XM_011516370.1:c.1231+9_1231+11del XP_011514672.1:n.1231+9_1231+11del
XM_011516371.1:c.135+9_135+11del XP_011514673.1:n.135+9_135+11del
XR_927487.1:n.1351+9_1351+11del
XM_011516370.3:c.1231+9_1231+11del XP_011514672.1:n.1231+9_1231+11del
XM_017012389.1:c.1231+9_1231+11del XP_016867878.1:n.1231+9_1231+11del
XM_017012390.1:c.1129+9_1129+11del XP_016867879.1:n.1129+9_1129+11del
XR_001744830.1:n.1353+9_1353+11del
NM_001166135.2:c.706+9_706+11del NP_001159607.1:n.706+9_706+11del
NM_018077.3:c.1129+9_1129+11del MANE Select NP_060547.2:n.1129+9_1129+11del