Canonical Allele Identifier: CA359512006

Gene: NIPBL

Linked Data

• MyVariant Identifiers: chr5:g.37052645C>A (hg19) ; chr5:g.37052543C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37052543C>A , CM000667.2:g.37052543C>A	GRCh38
NC_000005.9:g.37052645C>A , CM000667.1:g.37052645C>A	GRCh37
NC_000005.8:g.37088402C>A	NCBI36
NG_006987.1:g.180661C>A
NG_006987.2:g.180661C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.7240C>A MANE Select	ENSP00000282516.8:p.Leu2414Ile
ENST00000652901.1:c.7240C>A	ENSP00000499536.1:p.Leu2414Ile
ENST00000282516.12:c.7240C>A	ENSP00000282516.8:p.Leu2414Ile
ENST00000448238.2:c.7240C>A	ENSP00000406266.2:p.Leu2414Ile
ENST00000514335.1:n.1122C>A
ENST00000621733.1:c.1-12035C>A	ENSP00000480694.1:n.1-12035C>A
NM_015384.4:c.7240C>A	NP_056199.2:p.Leu2414Ile
NM_133433.3:c.7240C>A	NP_597677.2:p.Leu2414Ile
XM_005248280.2:c.7240C>A	XP_005248337.1:p.Leu2414Ile
XM_005248282.3:c.6496C>A	XP_005248339.2:p.Leu2166Ile
XM_006714467.2:c.7240C>A	XP_006714530.1:p.Leu2414Ile
XM_006714468.1:c.7042C>A	XP_006714531.1:p.Leu2348Ile
XM_011514014.1:c.6859C>A	XP_011512316.1:p.Leu2287Ile
XM_011514015.1:c.7240C>A	XP_011512317.1:p.Leu2414Ile
XM_005248280.3:c.7240C>A	XP_005248337.1:p.Leu2414Ile
XM_005248282.5:c.6580C>A	XP_005248339.3:p.Leu2194Ile
XM_006714468.2:c.7042C>A	XP_006714531.1:p.Leu2348Ile
XM_017009329.1:c.7240C>A	XP_016864818.1:p.Leu2414Ile
XM_017009330.2:c.5623C>A	XP_016864819.1:p.Leu1875Ile
XM_017009331.1:c.5614C>A	XP_016864820.1:p.Leu1872Ile
NM_133433.4:c.7240C>A MANE Select	NP_597677.2:p.Leu2414Ile
NM_015384.5:c.7240C>A	NP_056199.2:p.Leu2414Ile