Canonical Allele Identifier: CA1539572216

Gene: NIPBL

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37052436C= , CM000667.2:g.37052436C=	GRCh38
NC_000005.9:g.37052538C= , CM000667.1:g.37052538C=	GRCh37
NC_000005.8:g.37088295C=	NCBI36
NG_006987.1:g.180554C=
NG_006987.2:g.180554C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000282516.13:c.7133C= MANE Select	ENSP00000282516.8:p.Pro2378=
ENST00000652901.1:c.7133C=	ENSP00000499536.1:p.Pro2378=
ENST00000282516.12:c.7133C=	ENSP00000282516.8:p.Pro2378=
ENST00000448238.2:c.7133C=	ENSP00000406266.2:p.Pro2378=
ENST00000514335.1:n.1015C=
ENST00000621733.1:c.1-12142C=	ENSP00000480694.1:n.1-12142C=
NM_015384.4:c.7133C=	NP_056199.2:p.Pro2378=
NM_133433.3:c.7133C=	NP_597677.2:p.Pro2378=
XM_005248280.2:c.7133C=	XP_005248337.1:p.Pro2378=
XM_005248282.3:c.6389C=	XP_005248339.2:p.Pro2130=
XM_006714467.2:c.7133C=	XP_006714530.1:p.Pro2378=
XM_006714468.1:c.6935C=	XP_006714531.1:p.Pro2312=
XM_011514014.1:c.6752C=	XP_011512316.1:p.Pro2251=
XM_011514015.1:c.7133C=	XP_011512317.1:p.Pro2378=
XM_005248280.3:c.7133C=	XP_005248337.1:p.Pro2378=
XM_005248282.5:c.6473C=	XP_005248339.3:p.Pro2158=
XM_006714468.2:c.6935C=	XP_006714531.1:p.Pro2312=
XM_017009329.1:c.7133C=	XP_016864818.1:p.Pro2378=
XM_017009330.2:c.5516C=	XP_016864819.1:p.Pro1839=
XM_017009331.1:c.5507C=	XP_016864820.1:p.Pro1836=
NM_133433.4:c.7133C= MANE Select	NP_597677.2:p.Pro2378=
NM_015384.5:c.7133C=	NP_056199.2:p.Pro2378=