Canonical Allele Identifier: CA443901679

Gene: NIPBL

Linked Data

• MyVariant Identifiers: chr5:g.36953825C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36953723C>A , CM000667.2:g.36953723C>A	GRCh38
NC_000005.9:g.36953825C>A , CM000667.1:g.36953825C>A	GRCh37
NC_000005.8:g.36989582C>A	NCBI36
NG_006987.1:g.81841C>A
NG_006987.2:g.81841C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000282516.13:c.27C>A MANE Select	ENSP00000282516.8:p.Pro9=
ENST00000652901.1:c.27C>A	ENSP00000499536.1:p.Pro9=
ENST00000282516.12:c.27C>A	ENSP00000282516.8:p.Pro9=
ENST00000448238.2:c.27C>A	ENSP00000406266.2:p.Pro9=
ENST00000621733.1:c.-1+76701C>A	ENSP00000480694.1:n.-1+76701C>A
NM_015384.4:c.27C>A	NP_056199.2:p.Pro9=
NM_133433.3:c.27C>A	NP_597677.2:p.Pro9=
XM_005248280.2:c.27C>A	XP_005248337.1:p.Pro9=
XM_006714467.2:c.27C>A	XP_006714530.1:p.Pro9=
XM_006714468.1:c.27C>A	XP_006714531.1:p.Pro9=
XM_011514014.1:c.27C>A	XP_011512316.1:p.Pro9=
XM_011514015.1:c.27C>A	XP_011512317.1:p.Pro9=
XM_005248280.3:c.27C>A	XP_005248337.1:p.Pro9=
XM_006714468.2:c.27C>A	XP_006714531.1:p.Pro9=
XM_017009329.1:c.27C>A	XP_016864818.1:p.Pro9=
XM_017009331.1:c.27C>A	XP_016864820.1:p.Pro9=
NM_133433.4:c.27C>A MANE Select	NP_597677.2:p.Pro9=
NM_015384.5:c.27C>A	NP_056199.2:p.Pro9=