Canonical Allele Identifier: CA359519030

Gene: NIPBL

Linked Data

• MyVariant Identifiers: chr5:g.37061080C>A (hg19) ; chr5:g.37060978C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37060978C>A , CM000667.2:g.37060978C>A	GRCh38
NC_000005.9:g.37061080C>A , CM000667.1:g.37061080C>A	GRCh37
NC_000005.8:g.37096837C>A	NCBI36
NG_006987.1:g.189096C>A
NG_006987.2:g.189096C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.7820C>A MANE Select	ENSP00000282516.8:p.Thr2607Lys
ENST00000652901.1:c.7673C>A	ENSP00000499536.1:p.Thr2558Lys
ENST00000282516.12:c.7820C>A	ENSP00000282516.8:p.Thr2607Lys
ENST00000448238.2:c.7820C>A	ENSP00000406266.2:p.Thr2607Lys
ENST00000513819.1:c.263+1813C>A	ENSP00000421504.1:n.263+1813C>A
ENST00000514335.1:n.1702C>A
ENST00000621733.1:c.1-3600C>A	ENSP00000480694.1:n.1-3600C>A
NM_015384.4:c.7820C>A	NP_056199.2:p.Thr2607Lys
NM_133433.3:c.7820C>A	NP_597677.2:p.Thr2607Lys
XM_005248280.2:c.7820C>A	XP_005248337.1:p.Thr2607Lys
XM_005248282.3:c.7076C>A	XP_005248339.2:p.Thr2359Lys
XM_006714467.2:c.7673C>A	XP_006714530.1:p.Thr2558Lys
XM_006714468.1:c.7622C>A	XP_006714531.1:p.Thr2541Lys
XM_011514014.1:c.7439C>A	XP_011512316.1:p.Thr2480Lys
XM_005248280.3:c.7820C>A	XP_005248337.1:p.Thr2607Lys
XM_005248282.5:c.7160C>A	XP_005248339.3:p.Thr2387Lys
XM_006714468.2:c.7622C>A	XP_006714531.1:p.Thr2541Lys
XM_017009329.1:c.7673C>A	XP_016864818.1:p.Thr2558Lys
XM_017009330.2:c.6203C>A	XP_016864819.1:p.Thr2068Lys
XM_017009331.1:c.6194C>A	XP_016864820.1:p.Thr2065Lys
NM_133433.4:c.7820C>A MANE Select	NP_597677.2:p.Thr2607Lys
NM_015384.5:c.7820C>A	NP_056199.2:p.Thr2607Lys