Canonical Allele Identifier: CA444096523

Gene: NIPBL CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37064805C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37064703C>G , CM000667.2:g.37064703C>G	GRCh38
NC_000005.9:g.37064805C>G , CM000667.1:g.37064805C>G	GRCh37
NC_000005.8:g.37100562C>G	NCBI36
NG_006987.1:g.192821C>G
NG_006987.2:g.192821C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.8226C>G (NIPBL) MANE Select	ENSP00000282516.8:p.Gly2742=
ENST00000652901.1:c.*170C>G (NIPBL)	ENSP00000499536.1:n.*170C>G
ENST00000282516.12:c.8226C>G (NIPBL)	ENSP00000282516.8:p.Gly2742=
ENST00000514335.1:n.2149C>G (NIPBL)
ENST00000621733.1:c.126C>G (NIPBL)	ENSP00000480694.1:p.Gly42=
NM_015384.4:c.*680C>G (NIPBL)	NP_056199.2:n.*680C>G
NM_133433.3:c.8226C>G (NIPBL)	NP_597677.2:p.Gly2742=
XM_005248280.2:c.*170C>G (NIPBL)	XP_005248337.1:n.*170C>G
XM_005248282.3:c.7482C>G (NIPBL)	XP_005248339.2:p.Gly2494=
XM_006714467.2:c.8079C>G (NIPBL)	XP_006714530.1:p.Gly2693=
XM_006714468.1:c.8028C>G (NIPBL)	XP_006714531.1:p.Gly2676=
XM_011514014.1:c.7845C>G (NIPBL)	XP_011512316.1:p.Gly2615=
XM_005248280.3:c.*170C>G (NIPBL)	XP_005248337.1:n.*170C>G
XM_005248282.5:c.7566C>G (NIPBL)	XP_005248339.3:p.Gly2522=
XM_006714468.2:c.8028C>G (NIPBL)	XP_006714531.1:p.Gly2676=
XM_017009329.1:c.*170C>G (NIPBL)	XP_016864818.1:n.*170C>G
XM_017009330.2:c.6609C>G (NIPBL)	XP_016864819.1:p.Gly2203=
XM_017009331.1:c.6600C>G (NIPBL)	XP_016864820.1:p.Gly2200=
XR_925644.2:n.11979G>C (CPLANE1)
NM_133433.4:c.8226C>G (NIPBL) MANE Select	NP_597677.2:p.Gly2742=
NM_015384.5:c.*680C>G (NIPBL)	NP_056199.2:n.*680C>G