Canonical Allele Identifier: CA359510847

Gene: NIPBL

Linked Data

• MyVariant Identifiers: chr5:g.37051984T>A (hg19) ; chr5:g.37051882T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37051882T>A , CM000667.2:g.37051882T>A	GRCh38
NC_000005.9:g.37051984T>A , CM000667.1:g.37051984T>A	GRCh37
NC_000005.8:g.37087741T>A	NCBI36
NG_006987.1:g.180000T>A
NG_006987.2:g.180000T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000282516.13:c.7058T>A MANE Select	ENSP00000282516.8:p.Ile2353Asn
ENST00000652901.1:c.7058T>A	ENSP00000499536.1:p.Ile2353Asn
ENST00000282516.12:c.7058T>A	ENSP00000282516.8:p.Ile2353Asn
ENST00000448238.2:c.7058T>A	ENSP00000406266.2:p.Ile2353Asn
ENST00000514335.1:n.940T>A
ENST00000621733.1:c.1-12696T>A	ENSP00000480694.1:n.1-12696T>A
NM_015384.4:c.7058T>A	NP_056199.2:p.Ile2353Asn
NM_133433.3:c.7058T>A	NP_597677.2:p.Ile2353Asn
XM_005248280.2:c.7058T>A	XP_005248337.1:p.Ile2353Asn
XM_005248282.3:c.6314T>A	XP_005248339.2:p.Ile2105Asn
XM_006714467.2:c.7058T>A	XP_006714530.1:p.Ile2353Asn
XM_006714468.1:c.6860T>A	XP_006714531.1:p.Ile2287Asn
XM_011514014.1:c.6677T>A	XP_011512316.1:p.Ile2226Asn
XM_011514015.1:c.7058T>A	XP_011512317.1:p.Ile2353Asn
XM_005248280.3:c.7058T>A	XP_005248337.1:p.Ile2353Asn
XM_005248282.5:c.6398T>A	XP_005248339.3:p.Ile2133Asn
XM_006714468.2:c.6860T>A	XP_006714531.1:p.Ile2287Asn
XM_017009329.1:c.7058T>A	XP_016864818.1:p.Ile2353Asn
XM_017009330.2:c.5441T>A	XP_016864819.1:p.Ile1814Asn
XM_017009331.1:c.5432T>A	XP_016864820.1:p.Ile1811Asn
NM_133433.4:c.7058T>A MANE Select	NP_597677.2:p.Ile2353Asn
NM_015384.5:c.7058T>A	NP_056199.2:p.Ile2353Asn