Canonical Allele Identifier: CA359522615

Gene: NIPBL CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37064806T>A (hg19) ; chr5:g.37064704T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37064704T>A , CM000667.2:g.37064704T>A	GRCh38
NC_000005.9:g.37064806T>A , CM000667.1:g.37064806T>A	GRCh37
NC_000005.8:g.37100563T>A	NCBI36
NG_006987.1:g.192822T>A
NG_006987.2:g.192822T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.8227T>A (NIPBL) MANE Select	ENSP00000282516.8:p.Ser2743Thr
ENST00000652901.1:c.*171T>A (NIPBL)	ENSP00000499536.1:n.*171T>A
ENST00000282516.12:c.8227T>A (NIPBL)	ENSP00000282516.8:p.Ser2743Thr
ENST00000514335.1:n.2150T>A (NIPBL)
ENST00000621733.1:c.127T>A (NIPBL)	ENSP00000480694.1:p.Ser43Thr
NM_015384.4:c.*681T>A (NIPBL)	NP_056199.2:n.*681T>A
NM_133433.3:c.8227T>A (NIPBL)	NP_597677.2:p.Ser2743Thr
XM_005248280.2:c.*171T>A (NIPBL)	XP_005248337.1:n.*171T>A
XM_005248282.3:c.7483T>A (NIPBL)	XP_005248339.2:p.Ser2495Thr
XM_006714467.2:c.8080T>A (NIPBL)	XP_006714530.1:p.Ser2694Thr
XM_006714468.1:c.8029T>A (NIPBL)	XP_006714531.1:p.Ser2677Thr
XM_011514014.1:c.7846T>A (NIPBL)	XP_011512316.1:p.Ser2616Thr
XM_005248280.3:c.*171T>A (NIPBL)	XP_005248337.1:n.*171T>A
XM_005248282.5:c.7567T>A (NIPBL)	XP_005248339.3:p.Ser2523Thr
XM_006714468.2:c.8029T>A (NIPBL)	XP_006714531.1:p.Ser2677Thr
XM_017009329.1:c.*171T>A (NIPBL)	XP_016864818.1:n.*171T>A
XM_017009330.2:c.6610T>A (NIPBL)	XP_016864819.1:p.Ser2204Thr
XM_017009331.1:c.6601T>A (NIPBL)	XP_016864820.1:p.Ser2201Thr
XR_925644.2:n.11978A>T (CPLANE1)
NM_133433.4:c.8227T>A (NIPBL) MANE Select	NP_597677.2:p.Ser2743Thr
NM_015384.5:c.*681T>A (NIPBL)	NP_056199.2:n.*681T>A