Canonical Allele Identifier: CA1539582017

Gene: NIPBL

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36985537C= , CM000667.2:g.36985537C=	GRCh38
NC_000005.9:g.36985639C= , CM000667.1:g.36985639C=	GRCh37
NC_000005.8:g.37021396C=	NCBI36
NG_006987.1:g.113655C=
NG_006987.2:g.113655C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.2357C= MANE Select	ENSP00000282516.8:p.Thr786=
ENST00000652901.1:c.2357C=	ENSP00000499536.1:p.Thr786=
ENST00000282516.12:c.2357C=	ENSP00000282516.8:p.Thr786=
ENST00000448238.2:c.2357C=	ENSP00000406266.2:p.Thr786=
ENST00000504430.5:n.1977C=
ENST00000621733.1:c.1-79041C=	ENSP00000480694.1:n.1-79041C=
NM_015384.4:c.2357C=	NP_056199.2:p.Thr786=
NM_133433.3:c.2357C=	NP_597677.2:p.Thr786=
XM_005248280.2:c.2357C=	XP_005248337.1:p.Thr786=
XM_005248282.3:c.1613C=	XP_005248339.2:p.Thr538=
XM_006714467.2:c.2357C=	XP_006714530.1:p.Thr786=
XM_006714468.1:c.2357C=	XP_006714531.1:p.Thr786=
XM_011514014.1:c.2357C=	XP_011512316.1:p.Thr786=
XM_011514015.1:c.2357C=	XP_011512317.1:p.Thr786=
XM_005248280.3:c.2357C=	XP_005248337.1:p.Thr786=
XM_005248282.5:c.1697C=	XP_005248339.3:p.Thr566=
XM_006714468.2:c.2357C=	XP_006714531.1:p.Thr786=
XM_017009329.1:c.2357C=	XP_016864818.1:p.Thr786=
XM_017009330.2:c.740C=	XP_016864819.1:p.Thr247=
XM_017009331.1:c.1495+9135C=	XP_016864820.1:n.1495+9135C=
NM_133433.4:c.2357C= MANE Select	NP_597677.2:p.Thr786=
NM_015384.5:c.2357C=	NP_056199.2:p.Thr786=