Canonical Allele Identifier: CA444096353

Gene: NIPBL

Linked Data

• MyVariant Identifiers: chr5:g.36986279T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36986177T>A , CM000667.2:g.36986177T>A	GRCh38
NC_000005.9:g.36986279T>A , CM000667.1:g.36986279T>A	GRCh37
NC_000005.8:g.37022036T>A	NCBI36
NG_006987.1:g.114295T>A
NG_006987.2:g.114295T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.2997T>A MANE Select	ENSP00000282516.8:p.Ala999=
ENST00000652901.1:c.2997T>A	ENSP00000499536.1:p.Ala999=
ENST00000282516.12:c.2997T>A	ENSP00000282516.8:p.Ala999=
ENST00000448238.2:c.2997T>A	ENSP00000406266.2:p.Ala999=
ENST00000504430.5:n.2617T>A
ENST00000621733.1:c.1-78401T>A	ENSP00000480694.1:n.1-78401T>A
NM_015384.4:c.2997T>A	NP_056199.2:p.Ala999=
NM_133433.3:c.2997T>A	NP_597677.2:p.Ala999=
XM_005248280.2:c.2997T>A	XP_005248337.1:p.Ala999=
XM_005248282.3:c.2253T>A	XP_005248339.2:p.Ala751=
XM_006714467.2:c.2997T>A	XP_006714530.1:p.Ala999=
XM_006714468.1:c.2997T>A	XP_006714531.1:p.Ala999=
XM_011514014.1:c.2997T>A	XP_011512316.1:p.Ala999=
XM_011514015.1:c.2997T>A	XP_011512317.1:p.Ala999=
XM_005248280.3:c.2997T>A	XP_005248337.1:p.Ala999=
XM_005248282.5:c.2337T>A	XP_005248339.3:p.Ala779=
XM_006714468.2:c.2997T>A	XP_006714531.1:p.Ala999=
XM_017009329.1:c.2997T>A	XP_016864818.1:p.Ala999=
XM_017009330.2:c.1380T>A	XP_016864819.1:p.Ala460=
XM_017009331.1:c.1496-9445T>A	XP_016864820.1:n.1496-9445T>A
NM_133433.4:c.2997T>A MANE Select	NP_597677.2:p.Ala999=
NM_015384.5:c.2997T>A	NP_056199.2:p.Ala999=