Canonical Allele Identifier: CA359521930

Gene: NIPBL CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37064663C>G (hg19) ; chr5:g.37064561C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37064561C>G , CM000667.2:g.37064561C>G	GRCh38
NC_000005.9:g.37064663C>G , CM000667.1:g.37064663C>G	GRCh37
NC_000005.8:g.37100420C>G	NCBI36
NG_006987.1:g.192679C>G
NG_006987.2:g.192679C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.8084C>G (NIPBL) MANE Select	ENSP00000282516.8:p.Thr2695Arg
ENST00000652901.1:c.*28C>G (NIPBL)	ENSP00000499536.1:n.*28C>G
ENST00000282516.12:c.8084C>G (NIPBL)	ENSP00000282516.8:p.Thr2695Arg
ENST00000514335.1:n.2007C>G (NIPBL)
ENST00000621733.1:c.1-17C>G (NIPBL)	ENSP00000480694.1:n.1-17C>G
NM_015384.4:c.*538C>G (NIPBL)	NP_056199.2:n.*538C>G
NM_133433.3:c.8084C>G (NIPBL)	NP_597677.2:p.Thr2695Arg
XM_005248280.2:c.*28C>G (NIPBL)	XP_005248337.1:n.*28C>G
XM_005248282.3:c.7340C>G (NIPBL)	XP_005248339.2:p.Thr2447Arg
XM_006714467.2:c.7937C>G (NIPBL)	XP_006714530.1:p.Thr2646Arg
XM_006714468.1:c.7886C>G (NIPBL)	XP_006714531.1:p.Thr2629Arg
XM_011514014.1:c.7703C>G (NIPBL)	XP_011512316.1:p.Thr2568Arg
XM_005248280.3:c.*28C>G (NIPBL)	XP_005248337.1:n.*28C>G
XM_005248282.5:c.7424C>G (NIPBL)	XP_005248339.3:p.Thr2475Arg
XM_006714468.2:c.7886C>G (NIPBL)	XP_006714531.1:p.Thr2629Arg
XM_017009329.1:c.*28C>G (NIPBL)	XP_016864818.1:n.*28C>G
XM_017009330.2:c.6467C>G (NIPBL)	XP_016864819.1:p.Thr2156Arg
XM_017009331.1:c.6458C>G (NIPBL)	XP_016864820.1:p.Thr2153Arg
XR_925644.2:n.12121G>C (CPLANE1)
NM_133433.4:c.8084C>G (NIPBL) MANE Select	NP_597677.2:p.Thr2695Arg
NM_015384.5:c.*538C>G (NIPBL)	NP_056199.2:n.*538C>G