Canonical Allele Identifier: CA443909364

Gene: NIPBL

Linked Data

• MyVariant Identifiers: chr5:g.37051886G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37051784G>T , CM000667.2:g.37051784G>T	GRCh38
NC_000005.9:g.37051886G>T , CM000667.1:g.37051886G>T	GRCh37
NC_000005.8:g.37087643G>T	NCBI36
NG_006987.1:g.179902G>T
NG_006987.2:g.179902G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000282516.13:c.6960G>T MANE Select	ENSP00000282516.8:p.Val2320=
ENST00000652901.1:c.6960G>T	ENSP00000499536.1:p.Val2320=
ENST00000282516.12:c.6960G>T	ENSP00000282516.8:p.Val2320=
ENST00000448238.2:c.6960G>T	ENSP00000406266.2:p.Val2320=
ENST00000514335.1:n.842G>T
ENST00000621733.1:c.1-12794G>T	ENSP00000480694.1:n.1-12794G>T
NM_015384.4:c.6960G>T	NP_056199.2:p.Val2320=
NM_133433.3:c.6960G>T	NP_597677.2:p.Val2320=
XM_005248280.2:c.6960G>T	XP_005248337.1:p.Val2320=
XM_005248282.3:c.6216G>T	XP_005248339.2:p.Val2072=
XM_006714467.2:c.6960G>T	XP_006714530.1:p.Val2320=
XM_006714468.1:c.6762G>T	XP_006714531.1:p.Val2254=
XM_011514014.1:c.6579G>T	XP_011512316.1:p.Val2193=
XM_011514015.1:c.6960G>T	XP_011512317.1:p.Val2320=
XM_005248280.3:c.6960G>T	XP_005248337.1:p.Val2320=
XM_005248282.5:c.6300G>T	XP_005248339.3:p.Val2100=
XM_006714468.2:c.6762G>T	XP_006714531.1:p.Val2254=
XM_017009329.1:c.6960G>T	XP_016864818.1:p.Val2320=
XM_017009330.2:c.5343G>T	XP_016864819.1:p.Val1781=
XM_017009331.1:c.5334G>T	XP_016864820.1:p.Val1778=
NM_133433.4:c.6960G>T MANE Select	NP_597677.2:p.Val2320=
NM_015384.5:c.6960G>T	NP_056199.2:p.Val2320=