Canonical Allele Identifier: CA1539609350

Gene: NIPBL

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37010215C= , CM000667.2:g.37010215C=	GRCh38
NC_000005.9:g.37010317C= , CM000667.1:g.37010317C=	GRCh37
NC_000005.8:g.37046074C=	NCBI36
NG_006987.1:g.138333C=
NG_006987.2:g.138333C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.4550C= MANE Select	ENSP00000282516.8:p.Ser1517=
ENST00000652901.1:c.4550C=	ENSP00000499536.1:p.Ser1517=
ENST00000282516.12:c.4550C=	ENSP00000282516.8:p.Ser1517=
ENST00000448238.2:c.4550C=	ENSP00000406266.2:p.Ser1517=
ENST00000621733.1:c.1-54363C=	ENSP00000480694.1:n.1-54363C=
NM_015384.4:c.4550C=	NP_056199.2:p.Ser1517=
NM_133433.3:c.4550C=	NP_597677.2:p.Ser1517=
XM_005248280.2:c.4550C=	XP_005248337.1:p.Ser1517=
XM_005248282.3:c.3806C=	XP_005248339.2:p.Ser1269=
XM_006714467.2:c.4550C=	XP_006714530.1:p.Ser1517=
XM_006714468.1:c.4352C=	XP_006714531.1:p.Ser1451=
XM_011514014.1:c.4169C=	XP_011512316.1:p.Ser1390=
XM_011514015.1:c.4550C=	XP_011512317.1:p.Ser1517=
XM_005248280.3:c.4550C=	XP_005248337.1:p.Ser1517=
XM_005248282.5:c.3890C=	XP_005248339.3:p.Ser1297=
XM_006714468.2:c.4352C=	XP_006714531.1:p.Ser1451=
XM_017009329.1:c.4550C=	XP_016864818.1:p.Ser1517=
XM_017009330.2:c.2933C=	XP_016864819.1:p.Ser978=
XM_017009331.1:c.2924C=	XP_016864820.1:p.Ser975=
NM_133433.4:c.4550C= MANE Select	NP_597677.2:p.Ser1517=
NM_015384.5:c.4550C=	NP_056199.2:p.Ser1517=