Canonical Allele Identifier: CA1539582037

Gene: NIPBL

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36985554C= , CM000667.2:g.36985554C=	GRCh38
NC_000005.9:g.36985656C= , CM000667.1:g.36985656C=	GRCh37
NC_000005.8:g.37021413C=	NCBI36
NG_006987.1:g.113672C=
NG_006987.2:g.113672C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.2374C= MANE Select	ENSP00000282516.8:p.Arg792=
ENST00000652901.1:c.2374C=	ENSP00000499536.1:p.Arg792=
ENST00000282516.12:c.2374C=	ENSP00000282516.8:p.Arg792=
ENST00000448238.2:c.2374C=	ENSP00000406266.2:p.Arg792=
ENST00000504430.5:n.1994C=
ENST00000621733.1:c.1-79024C=	ENSP00000480694.1:n.1-79024C=
NM_015384.4:c.2374C=	NP_056199.2:p.Arg792=
NM_133433.3:c.2374C=	NP_597677.2:p.Arg792=
XM_005248280.2:c.2374C=	XP_005248337.1:p.Arg792=
XM_005248282.3:c.1630C=	XP_005248339.2:p.Arg544=
XM_006714467.2:c.2374C=	XP_006714530.1:p.Arg792=
XM_006714468.1:c.2374C=	XP_006714531.1:p.Arg792=
XM_011514014.1:c.2374C=	XP_011512316.1:p.Arg792=
XM_011514015.1:c.2374C=	XP_011512317.1:p.Arg792=
XM_005248280.3:c.2374C=	XP_005248337.1:p.Arg792=
XM_005248282.5:c.1714C=	XP_005248339.3:p.Arg572=
XM_006714468.2:c.2374C=	XP_006714531.1:p.Arg792=
XM_017009329.1:c.2374C=	XP_016864818.1:p.Arg792=
XM_017009330.2:c.757C=	XP_016864819.1:p.Arg253=
XM_017009331.1:c.1495+9152C=	XP_016864820.1:n.1495+9152C=
NM_133433.4:c.2374C= MANE Select	NP_597677.2:p.Arg792=
NM_015384.5:c.2374C=	NP_056199.2:p.Arg792=