Canonical Allele Identifier: CA1539614200

Gene: NIPBL

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37014681A= , CM000667.2:g.37014681A=	GRCh38
NC_000005.9:g.37014783A= , CM000667.1:g.37014783A=	GRCh37
NC_000005.8:g.37050540A=	NCBI36
NG_006987.1:g.142799A=
NG_006987.2:g.142799A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.4561-2A= MANE Select	ENSP00000282516.8:n.4561-2A=
ENST00000652901.1:c.4561-2A=	ENSP00000499536.1:n.4561-2A=
ENST00000282516.12:c.4561-2A=	ENSP00000282516.8:n.4561-2A=
ENST00000448238.2:c.4561-2A=	ENSP00000406266.2:n.4561-2A=
ENST00000621733.1:c.1-49897A=	ENSP00000480694.1:n.1-49897A=
NM_015384.4:c.4561-2A=	NP_056199.2:n.4561-2A=
NM_133433.3:c.4561-2A=	NP_597677.2:n.4561-2A=
XM_005248280.2:c.4561-2A=	XP_005248337.1:n.4561-2A=
XM_005248282.3:c.3817-2A=	XP_005248339.2:n.3817-2A=
XM_006714467.2:c.4561-2A=	XP_006714530.1:n.4561-2A=
XM_006714468.1:c.4363-2A=	XP_006714531.1:n.4363-2A=
XM_011514014.1:c.4180-2A=	XP_011512316.1:n.4180-2A=
XM_011514015.1:c.4561-2A=	XP_011512317.1:n.4561-2A=
XM_005248280.3:c.4561-2A=	XP_005248337.1:n.4561-2A=
XM_005248282.5:c.3901-2A=	XP_005248339.3:n.3901-2A=
XM_006714468.2:c.4363-2A=	XP_006714531.1:n.4363-2A=
XM_017009329.1:c.4561-2A=	XP_016864818.1:n.4561-2A=
XM_017009330.2:c.2944-2A=	XP_016864819.1:n.2944-2A=
XM_017009331.1:c.2935-2A=	XP_016864820.1:n.2935-2A=
NM_133433.4:c.4561-2A= MANE Select	NP_597677.2:n.4561-2A=
NM_015384.5:c.4561-2A=	NP_056199.2:n.4561-2A=