Canonical Allele Identifier: CA2695204303

Gene: NIPBL

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36976182_36976185del , CM000667.2:g.36976182_36976185del	GRCh38
NC_000005.9:g.36976284_36976287del , CM000667.1:g.36976284_36976287del	GRCh37
NC_000005.8:g.37012041_37012044del	NCBI36
NG_006987.1:g.104300_104303del
NG_006987.2:g.104300_104303del

Transcript Alleles

HGVS	Amino-acid change
ENST00000282516.13:c.1275_1278del MANE Select	ENSP00000282516.8:p.Thr426HisfsTer?
ENST00000652901.1:c.1275_1278del	ENSP00000499536.1:p.Thr426HisfsTer?
ENST00000282516.12:c.1275_1278del	ENSP00000282516.8:p.Thr426HisfsTer?
ENST00000448238.2:c.1275_1278del	ENSP00000406266.2:p.Thr426HisfsTer?
ENST00000504430.5:n.895_898del
ENST00000621733.1:c.1-88396_1-88393del	ENSP00000480694.1:n.1-88396_1-88393del
NM_015384.4:c.1275_1278del	NP_056199.2:p.Thr426HisfsTer?
NM_133433.3:c.1275_1278del	NP_597677.2:p.Thr426HisfsTer?
XM_005248280.2:c.1275_1278del	XP_005248337.1:p.Thr426HisfsTer?
XM_005248282.3:c.531_534del	XP_005248339.2:p.Thr178HisfsTer?
XM_006714467.2:c.1275_1278del	XP_006714530.1:p.Thr426HisfsTer?
XM_006714468.1:c.1275_1278del	XP_006714531.1:p.Thr426HisfsTer?
XM_011514014.1:c.1275_1278del	XP_011512316.1:p.Thr426HisfsTer?
XM_011514015.1:c.1275_1278del	XP_011512317.1:p.Thr426HisfsTer?
XM_005248280.3:c.1275_1278del	XP_005248337.1:p.Thr426HisfsTer?
XM_005248282.5:c.615_618del	XP_005248339.3:p.Thr206HisfsTer?
XM_006714468.2:c.1275_1278del	XP_006714531.1:p.Thr426HisfsTer?
XM_017009329.1:c.1275_1278del	XP_016864818.1:p.Thr426HisfsTer?
XM_017009331.1:c.1275_1278del	XP_016864820.1:p.Thr426HisfsTer?
NM_133433.4:c.1275_1278del MANE Select	NP_597677.2:p.Thr426HisfsTer?
NM_015384.5:c.1275_1278del	NP_056199.2:p.Thr426HisfsTer?