Canonical Allele Identifier: CA359489687

Gene: NIPBL

Linked Data

• dbSNP Id: rs1161575420
• gnomAD v2: 5-37022226-C-G
• gnomAD v4: 5-37022124-C-G
• MyVariant Identifiers: chr5:g.37022226C>G (hg19) ; chr5:g.37022124C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37022124C>G , CM000667.2:g.37022124C>G	GRCh38
NC_000005.9:g.37022226C>G , CM000667.1:g.37022226C>G	GRCh37
NC_000005.8:g.37057983C>G	NCBI36
NG_006987.1:g.150242C>G
NG_006987.2:g.150242C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.5402C>G MANE Select	ENSP00000282516.8:p.Ala1801Gly
ENST00000652901.1:c.5402C>G	ENSP00000499536.1:p.Ala1801Gly
ENST00000282516.12:c.5402C>G	ENSP00000282516.8:p.Ala1801Gly
ENST00000448238.2:c.5402C>G	ENSP00000406266.2:p.Ala1801Gly
ENST00000621733.1:c.1-42454C>G	ENSP00000480694.1:n.1-42454C>G
NM_015384.4:c.5402C>G	NP_056199.2:p.Ala1801Gly
NM_133433.3:c.5402C>G	NP_597677.2:p.Ala1801Gly
XM_005248280.2:c.5402C>G	XP_005248337.1:p.Ala1801Gly
XM_005248282.3:c.4658C>G	XP_005248339.2:p.Ala1553Gly
XM_006714467.2:c.5402C>G	XP_006714530.1:p.Ala1801Gly
XM_006714468.1:c.5204C>G	XP_006714531.1:p.Ala1735Gly
XM_011514014.1:c.5021C>G	XP_011512316.1:p.Ala1674Gly
XM_011514015.1:c.5402C>G	XP_011512317.1:p.Ala1801Gly
XM_005248280.3:c.5402C>G	XP_005248337.1:p.Ala1801Gly
XM_005248282.5:c.4742C>G	XP_005248339.3:p.Ala1581Gly
XM_006714468.2:c.5204C>G	XP_006714531.1:p.Ala1735Gly
XM_017009329.1:c.5402C>G	XP_016864818.1:p.Ala1801Gly
XM_017009330.2:c.3785C>G	XP_016864819.1:p.Ala1262Gly
XM_017009331.1:c.3776C>G	XP_016864820.1:p.Ala1259Gly
NM_133433.4:c.5402C>G MANE Select	NP_597677.2:p.Ala1801Gly
NM_015384.5:c.5402C>G	NP_056199.2:p.Ala1801Gly