Canonical Allele Identifier: CA2499217837

Gene: NIPBL

Linked Data

• ClinVar Variation Id: 1076298
• ClinVar RCV Id: RCV001390162
• dbSNP Id: rs2149644816

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36985387del , CM000667.2:g.36985387del	GRCh38
NC_000005.9:g.36985489del , CM000667.1:g.36985489del	GRCh37
NC_000005.8:g.37021246del	NCBI36
NG_006987.1:g.113505del
NG_006987.2:g.113505del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.2207del MANE Select	ENSP00000282516.8:p.Pro736GlnfsTer?
ENST00000652901.1:c.2207del	ENSP00000499536.1:p.Pro736GlnfsTer?
ENST00000282516.12:c.2207del	ENSP00000282516.8:p.Pro736GlnfsTer?
ENST00000448238.2:c.2207del	ENSP00000406266.2:p.Pro736GlnfsTer?
ENST00000504430.5:n.1827del
ENST00000621733.1:c.1-79191del	ENSP00000480694.1:n.1-79191del
NM_015384.4:c.2207del	NP_056199.2:p.Pro736GlnfsTer?
NM_133433.3:c.2207del	NP_597677.2:p.Pro736GlnfsTer?
XM_005248280.2:c.2207del	XP_005248337.1:p.Pro736GlnfsTer?
XM_005248282.3:c.1463del	XP_005248339.2:p.Pro488GlnfsTer?
XM_006714467.2:c.2207del	XP_006714530.1:p.Pro736GlnfsTer?
XM_006714468.1:c.2207del	XP_006714531.1:p.Pro736GlnfsTer?
XM_011514014.1:c.2207del	XP_011512316.1:p.Pro736GlnfsTer?
XM_011514015.1:c.2207del	XP_011512317.1:p.Pro736GlnfsTer?
XM_005248280.3:c.2207del	XP_005248337.1:p.Pro736GlnfsTer?
XM_005248282.5:c.1547del	XP_005248339.3:p.Pro516GlnfsTer?
XM_006714468.2:c.2207del	XP_006714531.1:p.Pro736GlnfsTer?
XM_017009329.1:c.2207del	XP_016864818.1:p.Pro736GlnfsTer?
XM_017009330.2:c.590del	XP_016864819.1:p.Pro197GlnfsTer?
XM_017009331.1:c.1495+8985del	XP_016864820.1:n.1495+8985del
NM_133433.4:c.2207del MANE Select	NP_597677.2:p.Pro736GlnfsTer?
NM_015384.5:c.2207del	NP_056199.2:p.Pro736GlnfsTer?