Canonical Allele Identifier: CA3235783

Gene: NIPBL

Linked Data

• ClinVar Variation Id: 907507
• ClinVar RCV Id: RCV001157401
• dbSNP Id: rs376768802
• ExAC: 5:36958288 A / G
• gnomAD v2: 5-36958288-A-G
• gnomAD v3: 5-36958186-A-G
• gnomAD v4: 5-36958186-A-G
• MyVariant Identifiers: chr5:g.36958288A>G (hg19) ; chr5:g.36958186A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36958186A>G , CM000667.2:g.36958186A>G	GRCh38
NC_000005.9:g.36958288A>G , CM000667.1:g.36958288A>G	GRCh37
NC_000005.8:g.36994045A>G	NCBI36
NG_006987.1:g.86304A>G
NG_006987.2:g.86304A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000282516.13:c.313A>G MANE Select	ENSP00000282516.8:p.Asn105Asp
ENST00000652901.1:c.313A>G	ENSP00000499536.1:p.Asn105Asp
ENST00000282516.12:c.313A>G	ENSP00000282516.8:p.Asn105Asp
ENST00000448238.2:c.313A>G	ENSP00000406266.2:p.Asn105Asp
ENST00000505998.5:n.292A>G
ENST00000621733.1:c.-1+81164A>G	ENSP00000480694.1:n.-1+81164A>G
NM_015384.4:c.313A>G	NP_056199.2:p.Asn105Asp
NM_133433.3:c.313A>G	NP_597677.2:p.Asn105Asp
XM_005248280.2:c.313A>G	XP_005248337.1:p.Asn105Asp
XM_006714467.2:c.313A>G	XP_006714530.1:p.Asn105Asp
XM_006714468.1:c.313A>G	XP_006714531.1:p.Asn105Asp
XM_011514014.1:c.313A>G	XP_011512316.1:p.Asn105Asp
XM_011514015.1:c.313A>G	XP_011512317.1:p.Asn105Asp
XM_005248280.3:c.313A>G	XP_005248337.1:p.Asn105Asp
XM_006714468.2:c.313A>G	XP_006714531.1:p.Asn105Asp
XM_017009329.1:c.313A>G	XP_016864818.1:p.Asn105Asp
XM_017009331.1:c.313A>G	XP_016864820.1:p.Asn105Asp
NM_133433.4:c.313A>G MANE Select	NP_597677.2:p.Asn105Asp
NM_015384.5:c.313A>G	NP_056199.2:p.Asn105Asp