Canonical Allele Identifier: CA2564883296
Gene: RBMS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.160357716_160357730del , CM000664.2:g.160357716_160357730del GRCh38
NC_000002.11:g.161214227_161214241del , CM000664.1:g.161214227_161214241del GRCh37
NC_000002.10:g.160922473_160922487del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000348849.8:c.251+9486_251+9500del MANE Select ENSP00000294904.6:n.251+9486_251+9500del
ENST00000348849.7:c.251+9486_251+9500del ENSP00000294904.6:n.251+9486_251+9500del
ENST00000392753.7:n.191+9486_191+9500del ENSP00000376508.4:n.191+9486_191+9500del
ENST00000409075.5:c.152+9486_152+9500del ENSP00000386347.1:n.152+9486_152+9500del
ENST00000409289.6:c.152+9486_152+9500del ENSP00000386571.2:n.152+9486_152+9500del
ENST00000409972.5:c.152+9486_152+9500del ENSP00000387280.1:n.152+9486_152+9500del
ENST00000428519.1:c.152+9486_152+9500del ENSP00000389016.1:n.152+9486_152+9500del
ENST00000474820.5:n.377+9486_377+9500del
ENST00000491781.5:n.370+9486_370+9500del
NM_002897.4:c.251+9486_251+9500del NP_002888.1:n.251+9486_251+9500del
NM_016836.3:c.251+9486_251+9500del NP_058520.1:n.251+9486_251+9500del
XM_005246737.1:c.251+9486_251+9500del XP_005246794.1:n.251+9486_251+9500del
XM_005246738.2:c.248+9486_248+9500del XP_005246795.1:n.248+9486_248+9500del
XM_005246739.2:c.245+9486_245+9500del XP_005246796.1:n.245+9486_245+9500del
XM_005246740.1:c.251+9486_251+9500del XP_005246797.1:n.251+9486_251+9500del
XM_005246741.3:c.242+9486_242+9500del XP_005246798.1:n.242+9486_242+9500del
XM_006712671.2:c.257+9486_257+9500del XP_006712734.1:n.257+9486_257+9500del
XM_006712672.2:c.257+9486_257+9500del XP_006712735.1:n.257+9486_257+9500del
XM_006712673.2:c.257+9486_257+9500del XP_006712736.1:n.257+9486_257+9500del
XM_006712674.2:c.257+9486_257+9500del XP_006712737.1:n.257+9486_257+9500del
XM_005246738.3:c.248+9486_248+9500del XP_005246795.1:n.248+9486_248+9500del
XM_017004626.2:c.248+9486_248+9500del XP_016860115.1:n.248+9486_248+9500del
XM_024453032.1:c.248+9486_248+9500del XP_024308800.1:n.248+9486_248+9500del
XM_024453033.1:c.245+9486_245+9500del XP_024308801.1:n.245+9486_245+9500del
XM_024453034.1:c.245+9486_245+9500del XP_024308802.1:n.245+9486_245+9500del
NM_016836.4:c.251+9486_251+9500del MANE Select NP_058520.1:n.251+9486_251+9500del
NM_002897.5:c.251+9486_251+9500del NP_002888.1:n.251+9486_251+9500del