Canonical Allele Identifier: CA1539590428

Gene: NIPBL CPLANE1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37064702G= , CM000667.2:g.37064702G=	GRCh38
NC_000005.9:g.37064804G= , CM000667.1:g.37064804G=	GRCh37
NC_000005.8:g.37100561G=	NCBI36
NG_006987.1:g.192820G=
NG_006987.2:g.192820G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.8225G= (NIPBL) MANE Select	ENSP00000282516.8:p.Gly2742=
ENST00000652901.1:c.*169G= (NIPBL)	ENSP00000499536.1:n.*169G=
ENST00000282516.12:c.8225G= (NIPBL)	ENSP00000282516.8:p.Gly2742=
ENST00000514335.1:n.2148G= (NIPBL)
ENST00000621733.1:c.125G= (NIPBL)	ENSP00000480694.1:p.Gly42=
NM_015384.4:c.*679G= (NIPBL)	NP_056199.2:n.*679G=
NM_133433.3:c.8225G= (NIPBL)	NP_597677.2:p.Gly2742=
XM_005248280.2:c.*169G= (NIPBL)	XP_005248337.1:n.*169G=
XM_005248282.3:c.7481G= (NIPBL)	XP_005248339.2:p.Gly2494=
XM_006714467.2:c.8078G= (NIPBL)	XP_006714530.1:p.Gly2693=
XM_006714468.1:c.8027G= (NIPBL)	XP_006714531.1:p.Gly2676=
XM_011514014.1:c.7844G= (NIPBL)	XP_011512316.1:p.Gly2615=
XM_005248280.3:c.*169G= (NIPBL)	XP_005248337.1:n.*169G=
XM_005248282.5:c.7565G= (NIPBL)	XP_005248339.3:p.Gly2522=
XM_006714468.2:c.8027G= (NIPBL)	XP_006714531.1:p.Gly2676=
XM_017009329.1:c.*169G= (NIPBL)	XP_016864818.1:n.*169G=
XM_017009330.2:c.6608G= (NIPBL)	XP_016864819.1:p.Gly2203=
XM_017009331.1:c.6599G= (NIPBL)	XP_016864820.1:p.Gly2200=
XR_925644.2:n.11980C= (CPLANE1)
NM_133433.4:c.8225G= (NIPBL) MANE Select	NP_597677.2:p.Gly2742=
NM_015384.5:c.*679G= (NIPBL)	NP_056199.2:n.*679G=