Canonical Allele Identifier: CA359522557

Gene: NIPBL CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37064789T>C (hg19) ; chr5:g.37064687T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37064687T>C , CM000667.2:g.37064687T>C	GRCh38
NC_000005.9:g.37064789T>C , CM000667.1:g.37064789T>C	GRCh37
NC_000005.8:g.37100546T>C	NCBI36
NG_006987.1:g.192805T>C
NG_006987.2:g.192805T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.8210T>C (NIPBL) MANE Select	ENSP00000282516.8:p.Val2737Ala
ENST00000652901.1:c.*154T>C (NIPBL)	ENSP00000499536.1:n.*154T>C
ENST00000282516.12:c.8210T>C (NIPBL)	ENSP00000282516.8:p.Val2737Ala
ENST00000514335.1:n.2133T>C (NIPBL)
ENST00000621733.1:c.110T>C (NIPBL)	ENSP00000480694.1:p.Val37Ala
NM_015384.4:c.*664T>C (NIPBL)	NP_056199.2:n.*664T>C
NM_133433.3:c.8210T>C (NIPBL)	NP_597677.2:p.Val2737Ala
XM_005248280.2:c.*154T>C (NIPBL)	XP_005248337.1:n.*154T>C
XM_005248282.3:c.7466T>C (NIPBL)	XP_005248339.2:p.Val2489Ala
XM_006714467.2:c.8063T>C (NIPBL)	XP_006714530.1:p.Val2688Ala
XM_006714468.1:c.8012T>C (NIPBL)	XP_006714531.1:p.Val2671Ala
XM_011514014.1:c.7829T>C (NIPBL)	XP_011512316.1:p.Val2610Ala
XM_005248280.3:c.*154T>C (NIPBL)	XP_005248337.1:n.*154T>C
XM_005248282.5:c.7550T>C (NIPBL)	XP_005248339.3:p.Val2517Ala
XM_006714468.2:c.8012T>C (NIPBL)	XP_006714531.1:p.Val2671Ala
XM_017009329.1:c.*154T>C (NIPBL)	XP_016864818.1:n.*154T>C
XM_017009330.2:c.6593T>C (NIPBL)	XP_016864819.1:p.Val2198Ala
XM_017009331.1:c.6584T>C (NIPBL)	XP_016864820.1:p.Val2195Ala
XR_925644.2:n.11995A>G (CPLANE1)
NM_133433.4:c.8210T>C (NIPBL) MANE Select	NP_597677.2:p.Val2737Ala
NM_015384.5:c.*664T>C (NIPBL)	NP_056199.2:n.*664T>C