Canonical Allele Identifier: CA1539603643

Gene: NIPBL

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37003225C= , CM000667.2:g.37003225C=	GRCh38
NC_000005.9:g.37003327C= , CM000667.1:g.37003327C=	GRCh37
NC_000005.8:g.37039084C=	NCBI36
NG_006987.1:g.131343C=
NG_006987.2:g.131343C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000282516.13:c.3769-36C= MANE Select	ENSP00000282516.8:n.3769-36C=
ENST00000652901.1:c.3769-36C=	ENSP00000499536.1:n.3769-36C=
ENST00000282516.12:c.3769-36C=	ENSP00000282516.8:n.3769-36C=
ENST00000448238.2:c.3769-36C=	ENSP00000406266.2:n.3769-36C=
ENST00000621733.1:c.1-61353C=	ENSP00000480694.1:n.1-61353C=
NM_015384.4:c.3769-36C=	NP_056199.2:n.3769-36C=
NM_133433.3:c.3769-36C=	NP_597677.2:n.3769-36C=
XM_005248280.2:c.3769-36C=	XP_005248337.1:n.3769-36C=
XM_005248282.3:c.3025-36C=	XP_005248339.2:n.3025-36C=
XM_006714467.2:c.3769-36C=	XP_006714530.1:n.3769-36C=
XM_006714468.1:c.3571-36C=	XP_006714531.1:n.3571-36C=
XM_011514014.1:c.3388-36C=	XP_011512316.1:n.3388-36C=
XM_011514015.1:c.3769-36C=	XP_011512317.1:n.3769-36C=
XM_005248280.3:c.3769-36C=	XP_005248337.1:n.3769-36C=
XM_005248282.5:c.3109-36C=	XP_005248339.3:n.3109-36C=
XM_006714468.2:c.3571-36C=	XP_006714531.1:n.3571-36C=
XM_017009329.1:c.3769-36C=	XP_016864818.1:n.3769-36C=
XM_017009330.2:c.2152-36C=	XP_016864819.1:n.2152-36C=
XM_017009331.1:c.2143-36C=	XP_016864820.1:n.2143-36C=
NM_133433.4:c.3769-36C= MANE Select	NP_597677.2:n.3769-36C=
NM_015384.5:c.3769-36C=	NP_056199.2:n.3769-36C=