Canonical Allele Identifier: CA1539568915

Gene: NIPBL

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36975801A= , CM000667.2:g.36975801A=	GRCh38
NC_000005.9:g.36975903A= , CM000667.1:g.36975903A=	GRCh37
NC_000005.8:g.37011660A=	NCBI36
NG_006987.1:g.103919A=
NG_006987.2:g.103919A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.894A= MANE Select	ENSP00000282516.8:p.Gln298=
ENST00000652901.1:c.894A=	ENSP00000499536.1:p.Gln298=
ENST00000282516.12:c.894A=	ENSP00000282516.8:p.Gln298=
ENST00000448238.2:c.894A=	ENSP00000406266.2:p.Gln298=
ENST00000504430.5:n.514A=
ENST00000505998.5:n.873A=
ENST00000621733.1:c.1-88777A=	ENSP00000480694.1:n.1-88777A=
NM_015384.4:c.894A=	NP_056199.2:p.Gln298=
NM_133433.3:c.894A=	NP_597677.2:p.Gln298=
XM_005248280.2:c.894A=	XP_005248337.1:p.Gln298=
XM_005248282.3:c.150A=	XP_005248339.2:p.Gln50=
XM_006714467.2:c.894A=	XP_006714530.1:p.Gln298=
XM_006714468.1:c.894A=	XP_006714531.1:p.Gln298=
XM_011514014.1:c.894A=	XP_011512316.1:p.Gln298=
XM_011514015.1:c.894A=	XP_011512317.1:p.Gln298=
XM_005248280.3:c.894A=	XP_005248337.1:p.Gln298=
XM_005248282.5:c.234A=	XP_005248339.3:p.Gln78=
XM_006714468.2:c.894A=	XP_006714531.1:p.Gln298=
XM_017009329.1:c.894A=	XP_016864818.1:p.Gln298=
XM_017009331.1:c.894A=	XP_016864820.1:p.Gln298=
NM_133433.4:c.894A= MANE Select	NP_597677.2:p.Gln298=
NM_015384.5:c.894A=	NP_056199.2:p.Gln298=