Canonical Allele Identifier: CA1302270660
Gene: RBMS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.160357640_160357641delinsAT , CM000664.2:g.160357640_160357641delinsAT GRCh38
NC_000002.11:g.161214151_161214152delinsAT , CM000664.1:g.161214151_161214152delinsAT GRCh37
NC_000002.10:g.160922397_160922398delinsAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000348849.8:c.251+9575_251+9576delinsAT MANE Select ENSP00000294904.6:n.251+9575_251+9576delinsAT
ENST00000348849.7:c.251+9575_251+9576delinsAT ENSP00000294904.6:n.251+9575_251+9576delinsAT
ENST00000392753.7:c.191+9575_191+9576delinsAT ENSP00000376508.4:n.191+9575_191+9576delinsAT
ENST00000409075.5:c.152+9575_152+9576delinsAT ENSP00000386347.1:n.152+9575_152+9576delinsAT
ENST00000409289.6:c.152+9575_152+9576delinsAT ENSP00000386571.2:n.152+9575_152+9576delinsAT
ENST00000409972.5:c.152+9575_152+9576delinsAT ENSP00000387280.1:n.152+9575_152+9576delinsAT
ENST00000428519.1:c.152+9575_152+9576delinsAT ENSP00000389016.1:n.152+9575_152+9576delinsAT
ENST00000474820.5:n.377+9575_377+9576delinsAT
ENST00000491781.5:n.370+9575_370+9576delinsAT
NM_002897.4:c.251+9575_251+9576delinsAT NP_002888.1:n.251+9575_251+9576delinsAT
NM_016836.3:c.251+9575_251+9576delinsAT NP_058520.1:n.251+9575_251+9576delinsAT
XM_005246737.1:c.251+9575_251+9576delinsAT XP_005246794.1:n.251+9575_251+9576delinsAT
XM_005246738.2:c.248+9575_248+9576delinsAT XP_005246795.1:n.248+9575_248+9576delinsAT
XM_005246739.2:c.245+9575_245+9576delinsAT XP_005246796.1:n.245+9575_245+9576delinsAT
XM_005246740.1:c.251+9575_251+9576delinsAT XP_005246797.1:n.251+9575_251+9576delinsAT
XM_005246741.3:c.242+9575_242+9576delinsAT XP_005246798.1:n.242+9575_242+9576delinsAT
XM_006712671.2:c.257+9575_257+9576delinsAT XP_006712734.1:n.257+9575_257+9576delinsAT
XM_006712672.2:c.257+9575_257+9576delinsAT XP_006712735.1:n.257+9575_257+9576delinsAT
XM_006712673.2:c.257+9575_257+9576delinsAT XP_006712736.1:n.257+9575_257+9576delinsAT
XM_006712674.2:c.257+9575_257+9576delinsAT XP_006712737.1:n.257+9575_257+9576delinsAT
XM_005246738.3:c.248+9575_248+9576delinsAT XP_005246795.1:n.248+9575_248+9576delinsAT
XM_017004626.2:c.248+9575_248+9576delinsAT XP_016860115.1:n.248+9575_248+9576delinsAT
XM_024453032.1:c.248+9575_248+9576delinsAT XP_024308800.1:n.248+9575_248+9576delinsAT
XM_024453033.1:c.245+9575_245+9576delinsAT XP_024308801.1:n.245+9575_245+9576delinsAT
XM_024453034.1:c.245+9575_245+9576delinsAT XP_024308802.1:n.245+9575_245+9576delinsAT
NM_016836.4:c.251+9575_251+9576delinsAT MANE Select NP_058520.1:n.251+9575_251+9576delinsAT
NM_002897.5:c.251+9575_251+9576delinsAT NP_002888.1:n.251+9575_251+9576delinsAT