Canonical Allele Identifier: CA277022

Gene: NIPBL

Linked Data

• ClinVar Variation Id: 211631
• ClinVar RCV Id: RCV000192791
• dbSNP Id: rs797045755
• MyVariant Identifiers: chr5:g.36958289dupA (hg19) ; chr5:g.36958187dupA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36958187dup , CM000667.2:g.36958187dup	GRCh38
NC_000005.9:g.36958289dup , CM000667.1:g.36958289dup	GRCh37
NC_000005.8:g.36994046dup	NCBI36
NG_006987.1:g.86305dup
NG_006987.2:g.86305dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.314dup MANE Select	ENSP00000282516.8:p.Asn105LysfsTer23
ENST00000652901.1:c.314dup	ENSP00000499536.1:p.Asn105LysfsTer23
ENST00000282516.12:c.314dup	ENSP00000282516.8:p.Asn105LysfsTer23
ENST00000448238.2:c.314dup	ENSP00000406266.2:p.Asn105LysfsTer23
ENST00000505998.5:n.293dup
ENST00000621733.1:c.-1+81165dup	ENSP00000480694.1:n.-1+81165dup
NM_015384.4:c.314dup	NP_056199.2:p.Asn105LysfsTer23
NM_133433.3:c.314dup	NP_597677.2:p.Asn105LysfsTer23
XM_005248280.2:c.314dup	XP_005248337.1:p.Asn105LysfsTer23
XM_006714467.2:c.314dup	XP_006714530.1:p.Asn105LysfsTer23
XM_006714468.1:c.314dup	XP_006714531.1:p.Asn105LysfsTer23
XM_011514014.1:c.314dup	XP_011512316.1:p.Asn105LysfsTer23
XM_011514015.1:c.314dup	XP_011512317.1:p.Asn105LysfsTer23
XM_005248280.3:c.314dup	XP_005248337.1:p.Asn105LysfsTer23
XM_006714468.2:c.314dup	XP_006714531.1:p.Asn105LysfsTer23
XM_017009329.1:c.314dup	XP_016864818.1:p.Asn105LysfsTer23
XM_017009331.1:c.314dup	XP_016864820.1:p.Asn105LysfsTer23
NM_133433.4:c.314dup MANE Select	NP_597677.2:p.Asn105LysfsTer23
NM_015384.5:c.314dup	NP_056199.2:p.Asn105LysfsTer23