Canonical Allele Identifier: CA1302270642
Gene: RBMS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.160357621_160357623delinsGCA , CM000664.2:g.160357621_160357623delinsGCA GRCh38
NC_000002.11:g.161214132_161214134delinsGCA , CM000664.1:g.161214132_161214134delinsGCA GRCh37
NC_000002.10:g.160922378_160922380delinsGCA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000348849.8:c.251+9593_251+9595delinsTGC MANE Select ENSP00000294904.6:n.251+9593_251+9595deli...
ENST00000348849.7:c.251+9593_251+9595delinsTGC ENSP00000294904.6:n.251+9593_251+9595deli...
ENST00000392753.7:c.191+9593_191+9595delinsTGC ENSP00000376508.4:n.191+9593_191+9595deli...
ENST00000409075.5:c.152+9593_152+9595delinsTGC ENSP00000386347.1:n.152+9593_152+9595deli...
ENST00000409289.6:c.152+9593_152+9595delinsTGC ENSP00000386571.2:n.152+9593_152+9595deli...
ENST00000409972.5:c.152+9593_152+9595delinsTGC ENSP00000387280.1:n.152+9593_152+9595deli...
ENST00000428519.1:c.152+9593_152+9595delinsTGC ENSP00000389016.1:n.152+9593_152+9595deli...
ENST00000474820.5:n.377+9593_377+9595delinsTGC
ENST00000491781.5:n.370+9593_370+9595delinsTGC
NM_002897.4:c.251+9593_251+9595delinsTGC NP_002888.1:n.251+9593_251+9595delinsTGC
NM_016836.3:c.251+9593_251+9595delinsTGC NP_058520.1:n.251+9593_251+9595delinsTGC
XM_005246737.1:c.251+9593_251+9595delinsTGC XP_005246794.1:n.251+9593_251+9595delinsT...
XM_005246738.2:c.248+9593_248+9595delinsTGC XP_005246795.1:n.248+9593_248+9595delinsT...
XM_005246739.2:c.245+9593_245+9595delinsTGC XP_005246796.1:n.245+9593_245+9595delinsT...
XM_005246740.1:c.251+9593_251+9595delinsTGC XP_005246797.1:n.251+9593_251+9595delinsT...
XM_005246741.3:c.242+9593_242+9595delinsTGC XP_005246798.1:n.242+9593_242+9595delinsT...
XM_006712671.2:c.257+9593_257+9595delinsTGC XP_006712734.1:n.257+9593_257+9595delinsT...
XM_006712672.2:c.257+9593_257+9595delinsTGC XP_006712735.1:n.257+9593_257+9595delinsT...
XM_006712673.2:c.257+9593_257+9595delinsTGC XP_006712736.1:n.257+9593_257+9595delinsT...
XM_006712674.2:c.257+9593_257+9595delinsTGC XP_006712737.1:n.257+9593_257+9595delinsT...
XM_005246738.3:c.248+9593_248+9595delinsTGC XP_005246795.1:n.248+9593_248+9595delinsT...
XM_017004626.2:c.248+9593_248+9595delinsTGC XP_016860115.1:n.248+9593_248+9595delinsT...
XM_024453032.1:c.248+9593_248+9595delinsTGC XP_024308800.1:n.248+9593_248+9595delinsT...
XM_024453033.1:c.245+9593_245+9595delinsTGC XP_024308801.1:n.245+9593_245+9595delinsT...
XM_024453034.1:c.245+9593_245+9595delinsTGC XP_024308802.1:n.245+9593_245+9595delinsT...
NM_016836.4:c.251+9593_251+9595delinsTGC MANE Select NP_058520.1:n.251+9593_251+9595delinsTGC
NM_002897.5:c.251+9593_251+9595delinsTGC NP_002888.1:n.251+9593_251+9595delinsTGC