Canonical Allele Identifier: CA3236010

Gene: NIPBL

Linked Data

• dbSNP Id: rs749708797
• ExAC: 5:36976302 A / G
• gnomAD v2: 5-36976302-A-G
• gnomAD v4: 5-36976200-A-G
• MyVariant Identifiers: chr5:g.36976302A>G (hg19) ; chr5:g.36976200A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36976200A>G , CM000667.2:g.36976200A>G	GRCh38
NC_000005.9:g.36976302A>G , CM000667.1:g.36976302A>G	GRCh37
NC_000005.8:g.37012059A>G	NCBI36
NG_006987.1:g.104318A>G
NG_006987.2:g.104318A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.1293A>G MANE Select	ENSP00000282516.8:p.Ala431=
ENST00000652901.1:c.1293A>G	ENSP00000499536.1:p.Ala431=
ENST00000282516.12:c.1293A>G	ENSP00000282516.8:p.Ala431=
ENST00000448238.2:c.1293A>G	ENSP00000406266.2:p.Ala431=
ENST00000504430.5:n.913A>G
ENST00000621733.1:c.1-88378A>G	ENSP00000480694.1:n.1-88378A>G
NM_015384.4:c.1293A>G	NP_056199.2:p.Ala431=
NM_133433.3:c.1293A>G	NP_597677.2:p.Ala431=
XM_005248280.2:c.1293A>G	XP_005248337.1:p.Ala431=
XM_005248282.3:c.549A>G	XP_005248339.2:p.Ala183=
XM_006714467.2:c.1293A>G	XP_006714530.1:p.Ala431=
XM_006714468.1:c.1293A>G	XP_006714531.1:p.Ala431=
XM_011514014.1:c.1293A>G	XP_011512316.1:p.Ala431=
XM_011514015.1:c.1293A>G	XP_011512317.1:p.Ala431=
XM_005248280.3:c.1293A>G	XP_005248337.1:p.Ala431=
XM_005248282.5:c.633A>G	XP_005248339.3:p.Ala211=
XM_006714468.2:c.1293A>G	XP_006714531.1:p.Ala431=
XM_017009329.1:c.1293A>G	XP_016864818.1:p.Ala431=
XM_017009331.1:c.1293A>G	XP_016864820.1:p.Ala431=
NM_133433.4:c.1293A>G MANE Select	NP_597677.2:p.Ala431=
NM_015384.5:c.1293A>G	NP_056199.2:p.Ala431=