Canonical Allele Identifier: CA224028

Gene: NIPBL

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37022256C>T , CM000667.2:g.37022256C>T	GRCh38
NC_000005.9:g.37022358C>T , CM000667.1:g.37022358C>T	GRCh37
NC_000005.8:g.37058115C>T	NCBI36
NG_006987.1:g.150374C>T
NG_006987.2:g.150374C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.5440C>T MANE Select	ENSP00000282516.8:p.Arg1814Ter
ENST00000652901.1:c.5440C>T	ENSP00000499536.1:p.Arg1814Ter
ENST00000282516.12:c.5440C>T	ENSP00000282516.8:p.Arg1814Ter
ENST00000448238.2:c.5440C>T	ENSP00000406266.2:p.Arg1814Ter
ENST00000621733.1:c.1-42322C>T	ENSP00000480694.1:n.1-42322C>T
NM_015384.4:c.5440C>T	NP_056199.2:p.Arg1814Ter
NM_133433.3:c.5440C>T	NP_597677.2:p.Arg1814Ter
XM_005248280.2:c.5440C>T	XP_005248337.1:p.Arg1814Ter
XM_005248282.3:c.4696C>T	XP_005248339.2:p.Arg1566Ter
XM_006714467.2:c.5440C>T	XP_006714530.1:p.Arg1814Ter
XM_006714468.1:c.5242C>T	XP_006714531.1:p.Arg1748Ter
XM_011514014.1:c.5059C>T	XP_011512316.1:p.Arg1687Ter
XM_011514015.1:c.5440C>T	XP_011512317.1:p.Arg1814Ter
XM_005248280.3:c.5440C>T	XP_005248337.1:p.Arg1814Ter
XM_005248282.5:c.4780C>T	XP_005248339.3:p.Arg1594Ter
XM_006714468.2:c.5242C>T	XP_006714531.1:p.Arg1748Ter
XM_017009329.1:c.5440C>T	XP_016864818.1:p.Arg1814Ter
XM_017009330.2:c.3823C>T	XP_016864819.1:p.Arg1275Ter
XM_017009331.1:c.3814C>T	XP_016864820.1:p.Arg1272Ter
NM_133433.4:c.5440C>T MANE Select	NP_597677.2:p.Arg1814Ter
NM_015384.5:c.5440C>T	NP_056199.2:p.Arg1814Ter