Canonical Allele Identifier: CA443905643

Gene: NIPBL

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37027361T>G , CM000667.2:g.37027361T>G	GRCh38
NC_000005.9:g.37027463T>G , CM000667.1:g.37027463T>G	GRCh37
NC_000005.8:g.37063220T>G	NCBI36
NG_006987.1:g.155479T>G
NG_006987.2:g.155479T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.5811T>G MANE Select	ENSP00000282516.8:p.Val1937=
ENST00000652901.1:c.5811T>G	ENSP00000499536.1:p.Val1937=
ENST00000282516.12:c.5811T>G	ENSP00000282516.8:p.Val1937=
ENST00000448238.2:c.5811T>G	ENSP00000406266.2:p.Val1937=
ENST00000621733.1:c.1-37217T>G	ENSP00000480694.1:n.1-37217T>G
NM_015384.4:c.5811T>G	NP_056199.2:p.Val1937=
NM_133433.3:c.5811T>G	NP_597677.2:p.Val1937=
XM_005248280.2:c.5811T>G	XP_005248337.1:p.Val1937=
XM_005248282.3:c.5067T>G	XP_005248339.2:p.Val1689=
XM_006714467.2:c.5811T>G	XP_006714530.1:p.Val1937=
XM_006714468.1:c.5613T>G	XP_006714531.1:p.Val1871=
XM_011514014.1:c.5430T>G	XP_011512316.1:p.Val1810=
XM_011514015.1:c.5811T>G	XP_011512317.1:p.Val1937=
XM_005248280.3:c.5811T>G	XP_005248337.1:p.Val1937=
XM_005248282.5:c.5151T>G	XP_005248339.3:p.Val1717=
XM_006714468.2:c.5613T>G	XP_006714531.1:p.Val1871=
XM_017009329.1:c.5811T>G	XP_016864818.1:p.Val1937=
XM_017009330.2:c.4194T>G	XP_016864819.1:p.Val1398=
XM_017009331.1:c.4185T>G	XP_016864820.1:p.Val1395=
NM_133433.4:c.5811T>G MANE Select	NP_597677.2:p.Val1937=
NM_015384.5:c.5811T>G	NP_056199.2:p.Val1937=