Canonical Allele Identifier: CA1539571478

Gene: NIPBL

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37051871T= , CM000667.2:g.37051871T=	GRCh38
NC_000005.9:g.37051973T= , CM000667.1:g.37051973T=	GRCh37
NC_000005.8:g.37087730T=	NCBI36
NG_006987.1:g.179989T=
NG_006987.2:g.179989T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000282516.13:c.7047T= MANE Select	ENSP00000282516.8:p.Tyr2349=
ENST00000652901.1:c.7047T=	ENSP00000499536.1:p.Tyr2349=
ENST00000282516.12:c.7047T=	ENSP00000282516.8:p.Tyr2349=
ENST00000448238.2:c.7047T=	ENSP00000406266.2:p.Tyr2349=
ENST00000514335.1:n.929T=
ENST00000621733.1:c.1-12707T=	ENSP00000480694.1:n.1-12707T=
NM_015384.4:c.7047T=	NP_056199.2:p.Tyr2349=
NM_133433.3:c.7047T=	NP_597677.2:p.Tyr2349=
XM_005248280.2:c.7047T=	XP_005248337.1:p.Tyr2349=
XM_005248282.3:c.6303T=	XP_005248339.2:p.Tyr2101=
XM_006714467.2:c.7047T=	XP_006714530.1:p.Tyr2349=
XM_006714468.1:c.6849T=	XP_006714531.1:p.Tyr2283=
XM_011514014.1:c.6666T=	XP_011512316.1:p.Tyr2222=
XM_011514015.1:c.7047T=	XP_011512317.1:p.Tyr2349=
XM_005248280.3:c.7047T=	XP_005248337.1:p.Tyr2349=
XM_005248282.5:c.6387T=	XP_005248339.3:p.Tyr2129=
XM_006714468.2:c.6849T=	XP_006714531.1:p.Tyr2283=
XM_017009329.1:c.7047T=	XP_016864818.1:p.Tyr2349=
XM_017009330.2:c.5430T=	XP_016864819.1:p.Tyr1810=
XM_017009331.1:c.5421T=	XP_016864820.1:p.Tyr1807=
NM_133433.4:c.7047T= MANE Select	NP_597677.2:p.Tyr2349=
NM_015384.5:c.7047T=	NP_056199.2:p.Tyr2349=