Canonical Allele Identifier: CA1539572281

Gene: NIPBL

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37052467T= , CM000667.2:g.37052467T=	GRCh38
NC_000005.9:g.37052569T= , CM000667.1:g.37052569T=	GRCh37
NC_000005.8:g.37088326T=	NCBI36
NG_006987.1:g.180585T=
NG_006987.2:g.180585T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.7164T= MANE Select	ENSP00000282516.8:p.Ser2388=
ENST00000652901.1:c.7164T=	ENSP00000499536.1:p.Ser2388=
ENST00000282516.12:c.7164T=	ENSP00000282516.8:p.Ser2388=
ENST00000448238.2:c.7164T=	ENSP00000406266.2:p.Ser2388=
ENST00000514335.1:n.1046T=
ENST00000621733.1:c.1-12111T=	ENSP00000480694.1:n.1-12111T=
NM_015384.4:c.7164T=	NP_056199.2:p.Ser2388=
NM_133433.3:c.7164T=	NP_597677.2:p.Ser2388=
XM_005248280.2:c.7164T=	XP_005248337.1:p.Ser2388=
XM_005248282.3:c.6420T=	XP_005248339.2:p.Ser2140=
XM_006714467.2:c.7164T=	XP_006714530.1:p.Ser2388=
XM_006714468.1:c.6966T=	XP_006714531.1:p.Ser2322=
XM_011514014.1:c.6783T=	XP_011512316.1:p.Ser2261=
XM_011514015.1:c.7164T=	XP_011512317.1:p.Ser2388=
XM_005248280.3:c.7164T=	XP_005248337.1:p.Ser2388=
XM_005248282.5:c.6504T=	XP_005248339.3:p.Ser2168=
XM_006714468.2:c.6966T=	XP_006714531.1:p.Ser2322=
XM_017009329.1:c.7164T=	XP_016864818.1:p.Ser2388=
XM_017009330.2:c.5547T=	XP_016864819.1:p.Ser1849=
XM_017009331.1:c.5538T=	XP_016864820.1:p.Ser1846=
NM_133433.4:c.7164T= MANE Select	NP_597677.2:p.Ser2388=
NM_015384.5:c.7164T=	NP_056199.2:p.Ser2388=