Canonical Allele Identifier: CA443916393

Gene: NIPBL CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37064647C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37064545C>A , CM000667.2:g.37064545C>A	GRCh38
NC_000005.9:g.37064647C>A , CM000667.1:g.37064647C>A	GRCh37
NC_000005.8:g.37100404C>A	NCBI36
NG_006987.1:g.192663C>A
NG_006987.2:g.192663C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.8068C>A (NIPBL) MANE Select	ENSP00000282516.8:p.Arg2690=
ENST00000652901.1:c.*12C>A (NIPBL)	ENSP00000499536.1:n.*12C>A
ENST00000282516.12:c.8068C>A (NIPBL)	ENSP00000282516.8:p.Arg2690=
ENST00000514335.1:n.1991C>A (NIPBL)
ENST00000621733.1:c.1-33C>A (NIPBL)	ENSP00000480694.1:n.1-33C>A
NM_015384.4:c.*522C>A (NIPBL)	NP_056199.2:n.*522C>A
NM_133433.3:c.8068C>A (NIPBL)	NP_597677.2:p.Arg2690=
XM_005248280.2:c.*12C>A (NIPBL)	XP_005248337.1:n.*12C>A
XM_005248282.3:c.7324C>A (NIPBL)	XP_005248339.2:p.Arg2442=
XM_006714467.2:c.7921C>A (NIPBL)	XP_006714530.1:p.Arg2641=
XM_006714468.1:c.7870C>A (NIPBL)	XP_006714531.1:p.Arg2624=
XM_011514014.1:c.7687C>A (NIPBL)	XP_011512316.1:p.Arg2563=
XM_005248280.3:c.*12C>A (NIPBL)	XP_005248337.1:n.*12C>A
XM_005248282.5:c.7408C>A (NIPBL)	XP_005248339.3:p.Arg2470=
XM_006714468.2:c.7870C>A (NIPBL)	XP_006714531.1:p.Arg2624=
XM_017009329.1:c.*12C>A (NIPBL)	XP_016864818.1:n.*12C>A
XM_017009330.2:c.6451C>A (NIPBL)	XP_016864819.1:p.Arg2151=
XM_017009331.1:c.6442C>A (NIPBL)	XP_016864820.1:p.Arg2148=
XR_925644.2:n.12137G>T (CPLANE1)
NM_133433.4:c.8068C>A (NIPBL) MANE Select	NP_597677.2:p.Arg2690=
NM_015384.5:c.*522C>A (NIPBL)	NP_056199.2:n.*522C>A