Canonical Allele Identifier: CA1539611471

Gene: NIPBL

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37038611A= , CM000667.2:g.37038611A=	GRCh38
NC_000005.9:g.37038713A= , CM000667.1:g.37038713A=	GRCh37
NC_000005.8:g.37074470A=	NCBI36
NG_006987.1:g.166729A=
NG_006987.2:g.166729A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.5981A= MANE Select	ENSP00000282516.8:p.Asn1994=
ENST00000652901.1:c.5981A=	ENSP00000499536.1:p.Asn1994=
ENST00000282516.12:c.5981A=	ENSP00000282516.8:p.Asn1994=
ENST00000448238.2:c.5981A=	ENSP00000406266.2:p.Asn1994=
ENST00000621733.1:c.1-25967A=	ENSP00000480694.1:n.1-25967A=
NM_015384.4:c.5981A=	NP_056199.2:p.Asn1994=
NM_133433.3:c.5981A=	NP_597677.2:p.Asn1994=
XM_005248280.2:c.5981A=	XP_005248337.1:p.Asn1994=
XM_005248282.3:c.5237A=	XP_005248339.2:p.Asn1746=
XM_006714467.2:c.5981A=	XP_006714530.1:p.Asn1994=
XM_006714468.1:c.5783A=	XP_006714531.1:p.Asn1928=
XM_011514014.1:c.5600A=	XP_011512316.1:p.Asn1867=
XM_011514015.1:c.5981A=	XP_011512317.1:p.Asn1994=
XM_005248280.3:c.5981A=	XP_005248337.1:p.Asn1994=
XM_005248282.5:c.5321A=	XP_005248339.3:p.Asn1774=
XM_006714468.2:c.5783A=	XP_006714531.1:p.Asn1928=
XM_017009329.1:c.5981A=	XP_016864818.1:p.Asn1994=
XM_017009330.2:c.4364A=	XP_016864819.1:p.Asn1455=
XM_017009331.1:c.4355A=	XP_016864820.1:p.Asn1452=
NM_133433.4:c.5981A= MANE Select	NP_597677.2:p.Asn1994=
NM_015384.5:c.5981A=	NP_056199.2:p.Asn1994=