Canonical Allele Identifier: CA1539618553

Gene: NIPBL

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37045549A= , CM000667.2:g.37045549A=	GRCh38
NC_000005.9:g.37045651A= , CM000667.1:g.37045651A=	GRCh37
NC_000005.8:g.37081408A=	NCBI36
NG_006987.1:g.173667A=
NG_006987.2:g.173667A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.6450A= MANE Select	ENSP00000282516.8:p.Leu2150=
ENST00000652901.1:c.6450A=	ENSP00000499536.1:p.Leu2150=
ENST00000282516.12:c.6450A=	ENSP00000282516.8:p.Leu2150=
ENST00000448238.2:c.6450A=	ENSP00000406266.2:p.Leu2150=
ENST00000621733.1:c.1-19029A=	ENSP00000480694.1:n.1-19029A=
NM_015384.4:c.6450A=	NP_056199.2:p.Leu2150=
NM_133433.3:c.6450A=	NP_597677.2:p.Leu2150=
XM_005248280.2:c.6450A=	XP_005248337.1:p.Leu2150=
XM_005248282.3:c.5706A=	XP_005248339.2:p.Leu1902=
XM_006714467.2:c.6450A=	XP_006714530.1:p.Leu2150=
XM_006714468.1:c.6252A=	XP_006714531.1:p.Leu2084=
XM_011514014.1:c.6069A=	XP_011512316.1:p.Leu2023=
XM_011514015.1:c.6450A=	XP_011512317.1:p.Leu2150=
XM_005248280.3:c.6450A=	XP_005248337.1:p.Leu2150=
XM_005248282.5:c.5790A=	XP_005248339.3:p.Leu1930=
XM_006714468.2:c.6252A=	XP_006714531.1:p.Leu2084=
XM_017009329.1:c.6450A=	XP_016864818.1:p.Leu2150=
XM_017009330.2:c.4833A=	XP_016864819.1:p.Leu1611=
XM_017009331.1:c.4824A=	XP_016864820.1:p.Leu1608=
NM_133433.4:c.6450A= MANE Select	NP_597677.2:p.Leu2150=
NM_015384.5:c.6450A=	NP_056199.2:p.Leu2150=