Canonical Allele Identifier: CA1539537103

Gene: NIPBL

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36876779G= , CM000667.2:g.36876779G=	GRCh38
NC_000005.9:g.36876881G= , CM000667.1:g.36876881G=	GRCh37
NC_000005.8:g.36912638G=	NCBI36
NG_006987.1:g.4897G=
NG_006987.2:g.4897G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.-479G= MANE Select	ENSP00000282516.8:n.-479G=
ENST00000282516.12:c.-479G=	ENSP00000282516.8:n.-479G=
NM_015384.4:c.-479G=	NP_056199.2:n.-479G=
NM_133433.3:c.-479G=	NP_597677.2:n.-479G=
XM_005248280.2:c.-479G=	XP_005248337.1:n.-479G=
XM_006714467.2:c.-479G=	XP_006714530.1:n.-479G=
XM_006714468.1:c.-479G=	XP_006714531.1:n.-479G=
XM_011514014.1:c.-479G=	XP_011512316.1:n.-479G=
XM_011514015.1:c.-479G=	XP_011512317.1:n.-479G=
XM_005248280.3:c.-479G=	XP_005248337.1:n.-479G=
XM_006714468.2:c.-479G=	XP_006714531.1:n.-479G=
XM_017009329.1:c.-479G=	XP_016864818.1:n.-479G=
XM_017009331.1:c.-479G=	XP_016864820.1:n.-479G=
NM_133433.4:c.-479G= MANE Select	NP_597677.2:n.-479G=
NM_015384.5:c.-479G=	NP_056199.2:n.-479G=