Canonical Allele Identifier: CA1539585157

Gene: NIPBL

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37021046C= , CM000667.2:g.37021046C=	GRCh38
NC_000005.9:g.37021148C= , CM000667.1:g.37021148C=	GRCh37
NC_000005.8:g.37056905C=	NCBI36
NG_006987.1:g.149164C=
NG_006987.2:g.149164C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.5328+169C= MANE Select	ENSP00000282516.8:n.5328+169C=
ENST00000652901.1:c.5328+169C=	ENSP00000499536.1:n.5328+169C=
ENST00000282516.12:c.5328+169C=	ENSP00000282516.8:n.5328+169C=
ENST00000448238.2:c.5328+169C=	ENSP00000406266.2:n.5328+169C=
ENST00000621733.1:c.1-43532C=	ENSP00000480694.1:n.1-43532C=
NM_015384.4:c.5328+169C=	NP_056199.2:n.5328+169C=
NM_133433.3:c.5328+169C=	NP_597677.2:n.5328+169C=
XM_005248280.2:c.5328+169C=	XP_005248337.1:n.5328+169C=
XM_005248282.3:c.4584+169C=	XP_005248339.2:n.4584+169C=
XM_006714467.2:c.5328+169C=	XP_006714530.1:n.5328+169C=
XM_006714468.1:c.5130+169C=	XP_006714531.1:n.5130+169C=
XM_011514014.1:c.4947+169C=	XP_011512316.1:n.4947+169C=
XM_011514015.1:c.5328+169C=	XP_011512317.1:n.5328+169C=
XM_005248280.3:c.5328+169C=	XP_005248337.1:n.5328+169C=
XM_005248282.5:c.4668+169C=	XP_005248339.3:n.4668+169C=
XM_006714468.2:c.5130+169C=	XP_006714531.1:n.5130+169C=
XM_017009329.1:c.5328+169C=	XP_016864818.1:n.5328+169C=
XM_017009330.2:c.3711+169C=	XP_016864819.1:n.3711+169C=
XM_017009331.1:c.3702+169C=	XP_016864820.1:n.3702+169C=
NM_133433.4:c.5328+169C= MANE Select	NP_597677.2:n.5328+169C=
NM_015384.5:c.5328+169C=	NP_056199.2:n.5328+169C=