Canonical Allele Identifier: CA359504835

Gene: NIPBL

Linked Data

• MyVariant Identifiers: chr5:g.37045682T>A (hg19) ; chr5:g.37045580T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37045580T>A , CM000667.2:g.37045580T>A	GRCh38
NC_000005.9:g.37045682T>A , CM000667.1:g.37045682T>A	GRCh37
NC_000005.8:g.37081439T>A	NCBI36
NG_006987.1:g.173698T>A
NG_006987.2:g.173698T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.6481T>A MANE Select	ENSP00000282516.8:p.Phe2161Ile
ENST00000652901.1:c.6481T>A	ENSP00000499536.1:p.Phe2161Ile
ENST00000282516.12:c.6481T>A	ENSP00000282516.8:p.Phe2161Ile
ENST00000448238.2:c.6481T>A	ENSP00000406266.2:p.Phe2161Ile
ENST00000621733.1:c.1-18998T>A	ENSP00000480694.1:n.1-18998T>A
NM_015384.4:c.6481T>A	NP_056199.2:p.Phe2161Ile
NM_133433.3:c.6481T>A	NP_597677.2:p.Phe2161Ile
XM_005248280.2:c.6481T>A	XP_005248337.1:p.Phe2161Ile
XM_005248282.3:c.5737T>A	XP_005248339.2:p.Phe1913Ile
XM_006714467.2:c.6481T>A	XP_006714530.1:p.Phe2161Ile
XM_006714468.1:c.6283T>A	XP_006714531.1:p.Phe2095Ile
XM_011514014.1:c.6100T>A	XP_011512316.1:p.Phe2034Ile
XM_011514015.1:c.6481T>A	XP_011512317.1:p.Phe2161Ile
XM_005248280.3:c.6481T>A	XP_005248337.1:p.Phe2161Ile
XM_005248282.5:c.5821T>A	XP_005248339.3:p.Phe1941Ile
XM_006714468.2:c.6283T>A	XP_006714531.1:p.Phe2095Ile
XM_017009329.1:c.6481T>A	XP_016864818.1:p.Phe2161Ile
XM_017009330.2:c.4864T>A	XP_016864819.1:p.Phe1622Ile
XM_017009331.1:c.4855T>A	XP_016864820.1:p.Phe1619Ile
NM_133433.4:c.6481T>A MANE Select	NP_597677.2:p.Phe2161Ile
NM_015384.5:c.6481T>A	NP_056199.2:p.Phe2161Ile