Canonical Allele Identifier: CA359498931

Gene: NIPBL

Linked Data

• MyVariant Identifiers: chr5:g.37038840T>A (hg19) ; chr5:g.37038738T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37038738T>A , CM000667.2:g.37038738T>A	GRCh38
NC_000005.9:g.37038840T>A , CM000667.1:g.37038840T>A	GRCh37
NC_000005.8:g.37074597T>A	NCBI36
NG_006987.1:g.166856T>A
NG_006987.2:g.166856T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.6108T>A MANE Select	ENSP00000282516.8:p.Ser2036Arg
ENST00000652901.1:c.6108T>A	ENSP00000499536.1:p.Ser2036Arg
ENST00000282516.12:c.6108T>A	ENSP00000282516.8:p.Ser2036Arg
ENST00000448238.2:c.6108T>A	ENSP00000406266.2:p.Ser2036Arg
ENST00000621733.1:c.1-25840T>A	ENSP00000480694.1:n.1-25840T>A
NM_015384.4:c.6108T>A	NP_056199.2:p.Ser2036Arg
NM_133433.3:c.6108T>A	NP_597677.2:p.Ser2036Arg
XM_005248280.2:c.6108T>A	XP_005248337.1:p.Ser2036Arg
XM_005248282.3:c.5364T>A	XP_005248339.2:p.Ser1788Arg
XM_006714467.2:c.6108T>A	XP_006714530.1:p.Ser2036Arg
XM_006714468.1:c.5910T>A	XP_006714531.1:p.Ser1970Arg
XM_011514014.1:c.5727T>A	XP_011512316.1:p.Ser1909Arg
XM_011514015.1:c.6108T>A	XP_011512317.1:p.Ser2036Arg
XM_005248280.3:c.6108T>A	XP_005248337.1:p.Ser2036Arg
XM_005248282.5:c.5448T>A	XP_005248339.3:p.Ser1816Arg
XM_006714468.2:c.5910T>A	XP_006714531.1:p.Ser1970Arg
XM_017009329.1:c.6108T>A	XP_016864818.1:p.Ser2036Arg
XM_017009330.2:c.4491T>A	XP_016864819.1:p.Ser1497Arg
XM_017009331.1:c.4482T>A	XP_016864820.1:p.Ser1494Arg
NM_133433.4:c.6108T>A MANE Select	NP_597677.2:p.Ser2036Arg
NM_015384.5:c.6108T>A	NP_056199.2:p.Ser2036Arg