Canonical Allele Identifier: CA2840195381

Gene: NIPBL

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36976369del , CM000667.2:g.36976369del	GRCh38
NC_000005.9:g.36976471del , CM000667.1:g.36976471del	GRCh37
NC_000005.8:g.37012228del	NCBI36
NG_006987.1:g.104487del
NG_006987.2:g.104487del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.1462del MANE Select	ENSP00000282516.8:p.Arg488GlyfsTer15
ENST00000652901.1:c.1462del	ENSP00000499536.1:p.Arg488GlyfsTer15
ENST00000282516.12:c.1462del	ENSP00000282516.8:p.Arg488GlyfsTer15
ENST00000448238.2:c.1462del	ENSP00000406266.2:p.Arg488GlyfsTer15
ENST00000504430.5:n.1082del
ENST00000621733.1:c.1-88209del	ENSP00000480694.1:n.1-88209del
NM_015384.4:c.1462del	NP_056199.2:p.Arg488GlyfsTer15
NM_133433.3:c.1462del	NP_597677.2:p.Arg488GlyfsTer15
XM_005248280.2:c.1462del	XP_005248337.1:p.Arg488GlyfsTer15
XM_005248282.3:c.718del	XP_005248339.2:p.Arg240GlyfsTer15
XM_006714467.2:c.1462del	XP_006714530.1:p.Arg488GlyfsTer15
XM_006714468.1:c.1462del	XP_006714531.1:p.Arg488GlyfsTer15
XM_011514014.1:c.1462del	XP_011512316.1:p.Arg488GlyfsTer15
XM_011514015.1:c.1462del	XP_011512317.1:p.Arg488GlyfsTer15
XM_005248280.3:c.1462del	XP_005248337.1:p.Arg488GlyfsTer15
XM_005248282.5:c.802del	XP_005248339.3:p.Arg268GlyfsTer15
XM_006714468.2:c.1462del	XP_006714531.1:p.Arg488GlyfsTer15
XM_017009329.1:c.1462del	XP_016864818.1:p.Arg488GlyfsTer15
XM_017009331.1:c.1462del	XP_016864820.1:p.Arg488GlyfsTer14
NM_133433.4:c.1462del MANE Select	NP_597677.2:p.Arg488GlyfsTer15
NM_015384.5:c.1462del	NP_056199.2:p.Arg488GlyfsTer15