Canonical Allele Identifier: CA1539618494

Gene: NIPBL

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37045488A= , CM000667.2:g.37045488A=	GRCh38
NC_000005.9:g.37045590A= , CM000667.1:g.37045590A=	GRCh37
NC_000005.8:g.37081347A=	NCBI36
NG_006987.1:g.173606A=
NG_006987.2:g.173606A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000282516.13:c.6389A= MANE Select	ENSP00000282516.8:p.Asn2130=
ENST00000652901.1:c.6389A=	ENSP00000499536.1:p.Asn2130=
ENST00000282516.12:c.6389A=	ENSP00000282516.8:p.Asn2130=
ENST00000448238.2:c.6389A=	ENSP00000406266.2:p.Asn2130=
ENST00000621733.1:c.1-19090A=	ENSP00000480694.1:n.1-19090A=
NM_015384.4:c.6389A=	NP_056199.2:p.Asn2130=
NM_133433.3:c.6389A=	NP_597677.2:p.Asn2130=
XM_005248280.2:c.6389A=	XP_005248337.1:p.Asn2130=
XM_005248282.3:c.5645A=	XP_005248339.2:p.Asn1882=
XM_006714467.2:c.6389A=	XP_006714530.1:p.Asn2130=
XM_006714468.1:c.6191A=	XP_006714531.1:p.Asn2064=
XM_011514014.1:c.6008A=	XP_011512316.1:p.Asn2003=
XM_011514015.1:c.6389A=	XP_011512317.1:p.Asn2130=
XM_005248280.3:c.6389A=	XP_005248337.1:p.Asn2130=
XM_005248282.5:c.5729A=	XP_005248339.3:p.Asn1910=
XM_006714468.2:c.6191A=	XP_006714531.1:p.Asn2064=
XM_017009329.1:c.6389A=	XP_016864818.1:p.Asn2130=
XM_017009330.2:c.4772A=	XP_016864819.1:p.Asn1591=
XM_017009331.1:c.4763A=	XP_016864820.1:p.Asn1588=
NM_133433.4:c.6389A= MANE Select	NP_597677.2:p.Asn2130=
NM_015384.5:c.6389A=	NP_056199.2:p.Asn2130=