Canonical Allele Identifier: CA359482435

Gene: NIPBL

Linked Data

• MyVariant Identifiers: chr5:g.37016189T>G (hg19) ; chr5:g.37016087T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37016087T>G , CM000667.2:g.37016087T>G	GRCh38
NC_000005.9:g.37016189T>G , CM000667.1:g.37016189T>G	GRCh37
NC_000005.8:g.37051946T>G	NCBI36
NG_006987.1:g.144205T>G
NG_006987.2:g.144205T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.4693T>G MANE Select	ENSP00000282516.8:p.Phe1565Val
ENST00000652901.1:c.4693T>G	ENSP00000499536.1:p.Phe1565Val
ENST00000282516.12:c.4693T>G	ENSP00000282516.8:p.Phe1565Val
ENST00000448238.2:c.4693T>G	ENSP00000406266.2:p.Phe1565Val
ENST00000621733.1:c.1-48491T>G	ENSP00000480694.1:n.1-48491T>G
NM_015384.4:c.4693T>G	NP_056199.2:p.Phe1565Val
NM_133433.3:c.4693T>G	NP_597677.2:p.Phe1565Val
XM_005248280.2:c.4693T>G	XP_005248337.1:p.Phe1565Val
XM_005248282.3:c.3949T>G	XP_005248339.2:p.Phe1317Val
XM_006714467.2:c.4693T>G	XP_006714530.1:p.Phe1565Val
XM_006714468.1:c.4495T>G	XP_006714531.1:p.Phe1499Val
XM_011514014.1:c.4312T>G	XP_011512316.1:p.Phe1438Val
XM_011514015.1:c.4693T>G	XP_011512317.1:p.Phe1565Val
XM_005248280.3:c.4693T>G	XP_005248337.1:p.Phe1565Val
XM_005248282.5:c.4033T>G	XP_005248339.3:p.Phe1345Val
XM_006714468.2:c.4495T>G	XP_006714531.1:p.Phe1499Val
XM_017009329.1:c.4693T>G	XP_016864818.1:p.Phe1565Val
XM_017009330.2:c.3076T>G	XP_016864819.1:p.Phe1026Val
XM_017009331.1:c.3067T>G	XP_016864820.1:p.Phe1023Val
NM_133433.4:c.4693T>G MANE Select	NP_597677.2:p.Phe1565Val
NM_015384.5:c.4693T>G	NP_056199.2:p.Phe1565Val