Canonical Allele Identifier: CA2631065646

Gene: NUBP2 SPSB3

Linked Data

• gnomAD v4: 16-1787300-AGGCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1787303_1787306del , CM000678.2:g.1787303_1787306del	GRCh38
NC_000016.9:g.1837304_1837307del , CM000678.1:g.1837304_1837307del	GRCh37
NC_000016.8:g.1777305_1777308del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000262302.14:c.334+348_334+351del (NUBP2) MANE Select	ENSP00000262302.9:n.334+348_334+351del
ENST00000262302.13:c.334+348_334+351del (NUBP2)	ENSP00000262302.9:n.334+348_334+351del
ENST00000562263.5:c.154+348_154+351del (NUBP2)	ENSP00000456199.1:n.154+348_154+351del
ENST00000563136.5:c.353+348_353+351del (NUBP2)	ENSP00000454576.1:n.353+348_353+351del
ENST00000564227.5:c.802+348_802+351del (NUBP2)
ENST00000565134.5:c.334+348_334+351del (NUBP2)	ENSP00000454815.1:n.334+348_334+351del
ENST00000565603.5:n.460+348_460+351del (NUBP2)
ENST00000565987.5:c.154+348_154+351del (NUBP2)	ENSP00000455896.1:n.154+348_154+351del
ENST00000567700.5:n.872_875del (NUBP2)
ENST00000568287.5:c.598+348_598+351del (NUBP2)	ENSP00000454982.1:n.598+348_598+351del
ENST00000568706.1:c.-89-374_-89-371del (NUBP2)	ENSP00000460079.1:n.-89-374_-89-371del
ENST00000568834.5:c.136-374_136-371del (NUBP2)	ENSP00000456928.1:n.136-374_136-371del
ENST00000569769.1:c.-12-5809_-12-5806del (SPSB3)	ENSP00000455098.1:n.-12-5809_-12-5806del
ENST00000569898.5:c.136-374_136-371del (NUBP2)	ENSP00000456284.1:n.136-374_136-371del
NM_001284501.1:c.154+348_154+351del (NUBP2)	NP_001271430.1:n.154+348_154+351del
NM_001284502.1:c.-89-374_-89-371del (NUBP2)	NP_001271431.1:n.-89-374_-89-371del
NM_012225.3:c.334+348_334+351del (NUBP2)	NP_036357.1:n.334+348_334+351del
NR_104318.1:n.234-374_234-371del (NUBP2)
XM_005255027.1:c.154+348_154+351del (NUBP2)	XP_005255084.1:n.154+348_154+351del
XM_005255028.1:c.154+348_154+351del (NUBP2)	XP_005255085.1:n.154+348_154+351del
XM_005255030.1:c.-89-374_-89-371del (NUBP2)	XP_005255087.1:n.-89-374_-89-371del
XM_011522338.1:c.164-374_164-371del (NUBP2)	XP_011520640.1:n.164-374_164-371del
XM_005255027.3:c.154+348_154+351del (NUBP2)	XP_005255084.1:n.154+348_154+351del
XM_011522338.2:c.164-374_164-371del (NUBP2)	XP_011520640.1:n.164-374_164-371del
XM_017022831.1:c.154+348_154+351del (NUBP2)	XP_016878320.1:n.154+348_154+351del
XM_017022832.2:c.197-374_197-371del (NUBP2)	XP_016878321.1:n.197-374_197-371del
XM_024450135.1:c.154+348_154+351del (NUBP2)	XP_024305903.1:n.154+348_154+351del
NM_012225.4:c.334+348_334+351del (NUBP2) MANE Select	NP_036357.1:n.334+348_334+351del
NM_001284501.2:c.154+348_154+351del (NUBP2)	NP_001271430.1:n.154+348_154+351del
NM_001284502.2:c.-89-374_-89-371del (NUBP2)	NP_001271431.1:n.-89-374_-89-371del
NR_104318.2:n.197-374_197-371del (NUBP2)