Canonical Allele Identifier: CA444096510

Gene: NIPBL CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37064778T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37064676T>C , CM000667.2:g.37064676T>C	GRCh38
NC_000005.9:g.37064778T>C , CM000667.1:g.37064778T>C	GRCh37
NC_000005.8:g.37100535T>C	NCBI36
NG_006987.1:g.192794T>C
NG_006987.2:g.192794T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.8199T>C (NIPBL) MANE Select	ENSP00000282516.8:p.Ser2733=
ENST00000652901.1:c.*143T>C (NIPBL)	ENSP00000499536.1:n.*143T>C
ENST00000282516.12:c.8199T>C (NIPBL)	ENSP00000282516.8:p.Ser2733=
ENST00000514335.1:n.2122T>C (NIPBL)
ENST00000621733.1:c.99T>C (NIPBL)	ENSP00000480694.1:p.Ser33=
NM_015384.4:c.*653T>C (NIPBL)	NP_056199.2:n.*653T>C
NM_133433.3:c.8199T>C (NIPBL)	NP_597677.2:p.Ser2733=
XM_005248280.2:c.*143T>C (NIPBL)	XP_005248337.1:n.*143T>C
XM_005248282.3:c.7455T>C (NIPBL)	XP_005248339.2:p.Ser2485=
XM_006714467.2:c.8052T>C (NIPBL)	XP_006714530.1:p.Ser2684=
XM_006714468.1:c.8001T>C (NIPBL)	XP_006714531.1:p.Ser2667=
XM_011514014.1:c.7818T>C (NIPBL)	XP_011512316.1:p.Ser2606=
XM_005248280.3:c.*143T>C (NIPBL)	XP_005248337.1:n.*143T>C
XM_005248282.5:c.7539T>C (NIPBL)	XP_005248339.3:p.Ser2513=
XM_006714468.2:c.8001T>C (NIPBL)	XP_006714531.1:p.Ser2667=
XM_017009329.1:c.*143T>C (NIPBL)	XP_016864818.1:n.*143T>C
XM_017009330.2:c.6582T>C (NIPBL)	XP_016864819.1:p.Ser2194=
XM_017009331.1:c.6573T>C (NIPBL)	XP_016864820.1:p.Ser2191=
XR_925644.2:n.12006A>G (CPLANE1)
NM_133433.4:c.8199T>C (NIPBL) MANE Select	NP_597677.2:p.Ser2733=
NM_015384.5:c.*653T>C (NIPBL)	NP_056199.2:n.*653T>C