Canonical Allele Identifier: CA2631065272

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1787209del , CM000678.2:g.1787209del GRCh38
NC_000016.9:g.1837210del , CM000678.1:g.1837210del GRCh37
NC_000016.8:g.1777211del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262302.14:c.334+254del (NUBP2) MANE Select ENSP00000262302.9:n.334+254del
ENST00000262302.13:c.334+254del (NUBP2) ENSP00000262302.9:n.334+254del
ENST00000562263.5:c.154+254del (NUBP2) ENSP00000456199.1:n.154+254del
ENST00000563136.5:c.353+254del (NUBP2) ENSP00000454576.1:n.353+254del
ENST00000564227.5:c.802+254del (NUBP2)
ENST00000565134.5:c.334+254del (NUBP2) ENSP00000454815.1:n.334+254del
ENST00000565603.5:n.460+254del (NUBP2)
ENST00000565987.5:c.154+254del (NUBP2) ENSP00000455896.1:n.154+254del
ENST00000566090.5:n.653del (NUBP2)
ENST00000567700.5:n.778del (NUBP2)
ENST00000568287.5:c.598+254del (NUBP2) ENSP00000454982.1:n.598+254del
ENST00000568706.1:c.-89-468del (NUBP2) ENSP00000460079.1:n.-89-468del
ENST00000568834.5:c.136-468del (NUBP2) ENSP00000456928.1:n.136-468del
ENST00000569769.1:c.-12-5714del (SPSB3) ENSP00000455098.1:n.-12-5714del
ENST00000569898.5:c.136-468del (NUBP2) ENSP00000456284.1:n.136-468del
NM_001284501.1:c.154+254del (NUBP2) NP_001271430.1:n.154+254del
NM_001284502.1:c.-89-468del (NUBP2) NP_001271431.1:n.-89-468del
NM_012225.3:c.334+254del (NUBP2) NP_036357.1:n.334+254del
NR_104318.1:n.234-468del (NUBP2)
XM_005255027.1:c.154+254del (NUBP2) XP_005255084.1:n.154+254del
XM_005255028.1:c.154+254del (NUBP2) XP_005255085.1:n.154+254del
XM_005255030.1:c.-89-468del (NUBP2) XP_005255087.1:n.-89-468del
XM_011522338.1:c.164-468del (NUBP2) XP_011520640.1:n.164-468del
XM_005255027.3:c.154+254del (NUBP2) XP_005255084.1:n.154+254del
XM_011522338.2:c.164-468del (NUBP2) XP_011520640.1:n.164-468del
XM_017022831.1:c.154+254del (NUBP2) XP_016878320.1:n.154+254del
XM_017022832.2:c.197-468del (NUBP2) XP_016878321.1:n.197-468del
XM_024450135.1:c.154+254del (NUBP2) XP_024305903.1:n.154+254del
NM_012225.4:c.334+254del (NUBP2) MANE Select NP_036357.1:n.334+254del
NM_001284501.2:c.154+254del (NUBP2) NP_001271430.1:n.154+254del
NM_001284502.2:c.-89-468del (NUBP2) NP_001271431.1:n.-89-468del
NR_104318.2:n.197-468del (NUBP2)