Canonical Allele Identifier: CA443904472

Gene: NIPBL

Linked Data

• MyVariant Identifiers: chr5:g.37016224T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37016122T>G , CM000667.2:g.37016122T>G	GRCh38
NC_000005.9:g.37016224T>G , CM000667.1:g.37016224T>G	GRCh37
NC_000005.8:g.37051981T>G	NCBI36
NG_006987.1:g.144240T>G
NG_006987.2:g.144240T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.4728T>G MANE Select	ENSP00000282516.8:p.Pro1576=
ENST00000652901.1:c.4728T>G	ENSP00000499536.1:p.Pro1576=
ENST00000282516.12:c.4728T>G	ENSP00000282516.8:p.Pro1576=
ENST00000448238.2:c.4728T>G	ENSP00000406266.2:p.Pro1576=
ENST00000621733.1:c.1-48456T>G	ENSP00000480694.1:n.1-48456T>G
NM_015384.4:c.4728T>G	NP_056199.2:p.Pro1576=
NM_133433.3:c.4728T>G	NP_597677.2:p.Pro1576=
XM_005248280.2:c.4728T>G	XP_005248337.1:p.Pro1576=
XM_005248282.3:c.3984T>G	XP_005248339.2:p.Pro1328=
XM_006714467.2:c.4728T>G	XP_006714530.1:p.Pro1576=
XM_006714468.1:c.4530T>G	XP_006714531.1:p.Pro1510=
XM_011514014.1:c.4347T>G	XP_011512316.1:p.Pro1449=
XM_011514015.1:c.4728T>G	XP_011512317.1:p.Pro1576=
XM_005248280.3:c.4728T>G	XP_005248337.1:p.Pro1576=
XM_005248282.5:c.4068T>G	XP_005248339.3:p.Pro1356=
XM_006714468.2:c.4530T>G	XP_006714531.1:p.Pro1510=
XM_017009329.1:c.4728T>G	XP_016864818.1:p.Pro1576=
XM_017009330.2:c.3111T>G	XP_016864819.1:p.Pro1037=
XM_017009331.1:c.3102T>G	XP_016864820.1:p.Pro1034=
NM_133433.4:c.4728T>G MANE Select	NP_597677.2:p.Pro1576=
NM_015384.5:c.4728T>G	NP_056199.2:p.Pro1576=