Canonical Allele Identifier: CA359509089

Gene: NIPBL

Linked Data

• MyVariant Identifiers: chr5:g.37049384G>A (hg19) ; chr5:g.37049282G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37049282G>A , CM000667.2:g.37049282G>A	GRCh38
NC_000005.9:g.37049384G>A , CM000667.1:g.37049384G>A	GRCh37
NC_000005.8:g.37085141G>A	NCBI36
NG_006987.1:g.177400G>A
NG_006987.2:g.177400G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.6935G>A MANE Select	ENSP00000282516.8:p.Gly2312Asp
ENST00000652901.1:c.6935G>A	ENSP00000499536.1:p.Gly2312Asp
ENST00000282516.12:c.6935G>A	ENSP00000282516.8:p.Gly2312Asp
ENST00000448238.2:c.6935G>A	ENSP00000406266.2:p.Gly2312Asp
ENST00000621733.1:c.1-15296G>A	ENSP00000480694.1:n.1-15296G>A
NM_015384.4:c.6935G>A	NP_056199.2:p.Gly2312Asp
NM_133433.3:c.6935G>A	NP_597677.2:p.Gly2312Asp
XM_005248280.2:c.6935G>A	XP_005248337.1:p.Gly2312Asp
XM_005248282.3:c.6191G>A	XP_005248339.2:p.Gly2064Asp
XM_006714467.2:c.6935G>A	XP_006714530.1:p.Gly2312Asp
XM_006714468.1:c.6737G>A	XP_006714531.1:p.Gly2246Asp
XM_011514014.1:c.6554G>A	XP_011512316.1:p.Gly2185Asp
XM_011514015.1:c.6935G>A	XP_011512317.1:p.Gly2312Asp
XM_005248280.3:c.6935G>A	XP_005248337.1:p.Gly2312Asp
XM_005248282.5:c.6275G>A	XP_005248339.3:p.Gly2092Asp
XM_006714468.2:c.6737G>A	XP_006714531.1:p.Gly2246Asp
XM_017009329.1:c.6935G>A	XP_016864818.1:p.Gly2312Asp
XM_017009330.2:c.5318G>A	XP_016864819.1:p.Gly1773Asp
XM_017009331.1:c.5309G>A	XP_016864820.1:p.Gly1770Asp
NM_133433.4:c.6935G>A MANE Select	NP_597677.2:p.Gly2312Asp
NM_015384.5:c.6935G>A	NP_056199.2:p.Gly2312Asp