Canonical Allele Identifier: CA444096513

Gene: NIPBL CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37064781C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37064679C>T , CM000667.2:g.37064679C>T	GRCh38
NC_000005.9:g.37064781C>T , CM000667.1:g.37064781C>T	GRCh37
NC_000005.8:g.37100538C>T	NCBI36
NG_006987.1:g.192797C>T
NG_006987.2:g.192797C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.8202C>T (NIPBL) MANE Select	ENSP00000282516.8:p.Gly2734=
ENST00000652901.1:c.*146C>T (NIPBL)	ENSP00000499536.1:n.*146C>T
ENST00000282516.12:c.8202C>T (NIPBL)	ENSP00000282516.8:p.Gly2734=
ENST00000514335.1:n.2125C>T (NIPBL)
ENST00000621733.1:c.102C>T (NIPBL)	ENSP00000480694.1:p.Gly34=
NM_015384.4:c.*656C>T (NIPBL)	NP_056199.2:n.*656C>T
NM_133433.3:c.8202C>T (NIPBL)	NP_597677.2:p.Gly2734=
XM_005248280.2:c.*146C>T (NIPBL)	XP_005248337.1:n.*146C>T
XM_005248282.3:c.7458C>T (NIPBL)	XP_005248339.2:p.Gly2486=
XM_006714467.2:c.8055C>T (NIPBL)	XP_006714530.1:p.Gly2685=
XM_006714468.1:c.8004C>T (NIPBL)	XP_006714531.1:p.Gly2668=
XM_011514014.1:c.7821C>T (NIPBL)	XP_011512316.1:p.Gly2607=
XM_005248280.3:c.*146C>T (NIPBL)	XP_005248337.1:n.*146C>T
XM_005248282.5:c.7542C>T (NIPBL)	XP_005248339.3:p.Gly2514=
XM_006714468.2:c.8004C>T (NIPBL)	XP_006714531.1:p.Gly2668=
XM_017009329.1:c.*146C>T (NIPBL)	XP_016864818.1:n.*146C>T
XM_017009330.2:c.6585C>T (NIPBL)	XP_016864819.1:p.Gly2195=
XM_017009331.1:c.6576C>T (NIPBL)	XP_016864820.1:p.Gly2192=
XR_925644.2:n.12003G>A (CPLANE1)
NM_133433.4:c.8202C>T (NIPBL) MANE Select	NP_597677.2:p.Gly2734=
NM_015384.5:c.*656C>T (NIPBL)	NP_056199.2:n.*656C>T