Canonical Allele Identifier: CA915943359

Gene: NIPBL

Linked Data

• ClinVar Variation Id: 802112
• ClinVar RCV Id: RCV000987509
• dbSNP Id: rs1580323151

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36955633del , CM000667.2:g.36955633del	GRCh38
NC_000005.9:g.36955735del , CM000667.1:g.36955735del	GRCh37
NC_000005.8:g.36991492del	NCBI36
NG_006987.1:g.83751del
NG_006987.2:g.83751del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.226del MANE Select	ENSP00000282516.8:p.His76ThrfsTer2
ENST00000652901.1:c.226del	ENSP00000499536.1:p.His76ThrfsTer2
ENST00000282516.12:c.226del	ENSP00000282516.8:p.His76ThrfsTer2
ENST00000448238.2:c.226del	ENSP00000406266.2:p.His76ThrfsTer2
ENST00000505998.5:n.205del
ENST00000621733.1:c.-1+78611del	ENSP00000480694.1:n.-1+78611del
NM_015384.4:c.226del	NP_056199.2:p.His76ThrfsTer2
NM_133433.3:c.226del	NP_597677.2:p.His76ThrfsTer2
XM_005248280.2:c.226del	XP_005248337.1:p.His76ThrfsTer2
XM_006714467.2:c.226del	XP_006714530.1:p.His76ThrfsTer2
XM_006714468.1:c.226del	XP_006714531.1:p.His76ThrfsTer2
XM_011514014.1:c.226del	XP_011512316.1:p.His76ThrfsTer2
XM_011514015.1:c.226del	XP_011512317.1:p.His76ThrfsTer2
XM_005248280.3:c.226del	XP_005248337.1:p.His76ThrfsTer2
XM_006714468.2:c.226del	XP_006714531.1:p.His76ThrfsTer2
XM_017009329.1:c.226del	XP_016864818.1:p.His76ThrfsTer2
XM_017009331.1:c.226del	XP_016864820.1:p.His76ThrfsTer2
NM_133433.4:c.226del MANE Select	NP_597677.2:p.His76ThrfsTer2
NM_015384.5:c.226del	NP_056199.2:p.His76ThrfsTer2