Canonical Allele Identifier: CA359482769

Gene: NIPBL

Linked Data

• COSMIC: COSM3776667 ; COSM3776668
• MyVariant Identifiers: chr5:g.37016225G>A (hg19) ; chr5:g.37016123G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37016123G>A , CM000667.2:g.37016123G>A	GRCh38
NC_000005.9:g.37016225G>A , CM000667.1:g.37016225G>A	GRCh37
NC_000005.8:g.37051982G>A	NCBI36
NG_006987.1:g.144241G>A
NG_006987.2:g.144241G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.4729G>A MANE Select	ENSP00000282516.8:p.Glu1577Lys
ENST00000652901.1:c.4729G>A	ENSP00000499536.1:p.Glu1577Lys
ENST00000282516.12:c.4729G>A	ENSP00000282516.8:p.Glu1577Lys
ENST00000448238.2:c.4729G>A	ENSP00000406266.2:p.Glu1577Lys
ENST00000621733.1:c.1-48455G>A	ENSP00000480694.1:n.1-48455G>A
NM_015384.4:c.4729G>A	NP_056199.2:p.Glu1577Lys
NM_133433.3:c.4729G>A	NP_597677.2:p.Glu1577Lys
XM_005248280.2:c.4729G>A	XP_005248337.1:p.Glu1577Lys
XM_005248282.3:c.3985G>A	XP_005248339.2:p.Glu1329Lys
XM_006714467.2:c.4729G>A	XP_006714530.1:p.Glu1577Lys
XM_006714468.1:c.4531G>A	XP_006714531.1:p.Glu1511Lys
XM_011514014.1:c.4348G>A	XP_011512316.1:p.Glu1450Lys
XM_011514015.1:c.4729G>A	XP_011512317.1:p.Glu1577Lys
XM_005248280.3:c.4729G>A	XP_005248337.1:p.Glu1577Lys
XM_005248282.5:c.4069G>A	XP_005248339.3:p.Glu1357Lys
XM_006714468.2:c.4531G>A	XP_006714531.1:p.Glu1511Lys
XM_017009329.1:c.4729G>A	XP_016864818.1:p.Glu1577Lys
XM_017009330.2:c.3112G>A	XP_016864819.1:p.Glu1038Lys
XM_017009331.1:c.3103G>A	XP_016864820.1:p.Glu1035Lys
NM_133433.4:c.4729G>A MANE Select	NP_597677.2:p.Glu1577Lys
NM_015384.5:c.4729G>A	NP_056199.2:p.Glu1577Lys