Canonical Allele Identifier: CA117044362

Gene: NIPBL

Linked Data

• ClinVar Variation Id: 2867471
• ClinVar RCV Id: RCV003602645
• dbSNP Id: rs868508212
• MyVariant Identifiers: chr5:g.36985599A>G (hg19) ; chr5:g.36985497A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36985497A>G , CM000667.2:g.36985497A>G	GRCh38
NC_000005.9:g.36985599A>G , CM000667.1:g.36985599A>G	GRCh37
NC_000005.8:g.37021356A>G	NCBI36
NG_006987.1:g.113615A>G
NG_006987.2:g.113615A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000282516.13:c.2317A>G MANE Select	ENSP00000282516.8:p.Thr773Ala
ENST00000652901.1:c.2317A>G	ENSP00000499536.1:p.Thr773Ala
ENST00000282516.12:c.2317A>G	ENSP00000282516.8:p.Thr773Ala
ENST00000448238.2:c.2317A>G	ENSP00000406266.2:p.Thr773Ala
ENST00000504430.5:n.1937A>G
ENST00000621733.1:c.1-79081A>G	ENSP00000480694.1:n.1-79081A>G
NM_015384.4:c.2317A>G	NP_056199.2:p.Thr773Ala
NM_133433.3:c.2317A>G	NP_597677.2:p.Thr773Ala
XM_005248280.2:c.2317A>G	XP_005248337.1:p.Thr773Ala
XM_005248282.3:c.1573A>G	XP_005248339.2:p.Thr525Ala
XM_006714467.2:c.2317A>G	XP_006714530.1:p.Thr773Ala
XM_006714468.1:c.2317A>G	XP_006714531.1:p.Thr773Ala
XM_011514014.1:c.2317A>G	XP_011512316.1:p.Thr773Ala
XM_011514015.1:c.2317A>G	XP_011512317.1:p.Thr773Ala
XM_005248280.3:c.2317A>G	XP_005248337.1:p.Thr773Ala
XM_005248282.5:c.1657A>G	XP_005248339.3:p.Thr553Ala
XM_006714468.2:c.2317A>G	XP_006714531.1:p.Thr773Ala
XM_017009329.1:c.2317A>G	XP_016864818.1:p.Thr773Ala
XM_017009330.2:c.700A>G	XP_016864819.1:p.Thr234Ala
XM_017009331.1:c.1495+9095A>G	XP_016864820.1:n.1495+9095A>G
NM_133433.4:c.2317A>G MANE Select	NP_597677.2:p.Thr773Ala
NM_015384.5:c.2317A>G	NP_056199.2:p.Thr773Ala