Canonical Allele Identifier: CA443907825

Gene: NIPBL

Linked Data

• ClinVar Variation Id: 2916231
• ClinVar RCV Id: RCV003603999
• dbSNP Id: rs1297675054
• gnomAD v3: 5-37049139-A-G
• gnomAD v4: 5-37049139-A-G
• MyVariant Identifiers: chr5:g.37049241A>G (hg19) ; chr5:g.37049139A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37049139A>G , CM000667.2:g.37049139A>G	GRCh38
NC_000005.9:g.37049241A>G , CM000667.1:g.37049241A>G	GRCh37
NC_000005.8:g.37084998A>G	NCBI36
NG_006987.1:g.177257A>G
NG_006987.2:g.177257A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.6792A>G MANE Select	ENSP00000282516.8:p.Leu2264=
ENST00000652901.1:c.6792A>G	ENSP00000499536.1:p.Leu2264=
ENST00000282516.12:c.6792A>G	ENSP00000282516.8:p.Leu2264=
ENST00000448238.2:c.6792A>G	ENSP00000406266.2:p.Leu2264=
ENST00000621733.1:c.1-15439A>G	ENSP00000480694.1:n.1-15439A>G
NM_015384.4:c.6792A>G	NP_056199.2:p.Leu2264=
NM_133433.3:c.6792A>G	NP_597677.2:p.Leu2264=
XM_005248280.2:c.6792A>G	XP_005248337.1:p.Leu2264=
XM_005248282.3:c.6048A>G	XP_005248339.2:p.Leu2016=
XM_006714467.2:c.6792A>G	XP_006714530.1:p.Leu2264=
XM_006714468.1:c.6594A>G	XP_006714531.1:p.Leu2198=
XM_011514014.1:c.6411A>G	XP_011512316.1:p.Leu2137=
XM_011514015.1:c.6792A>G	XP_011512317.1:p.Leu2264=
XM_005248280.3:c.6792A>G	XP_005248337.1:p.Leu2264=
XM_005248282.5:c.6132A>G	XP_005248339.3:p.Leu2044=
XM_006714468.2:c.6594A>G	XP_006714531.1:p.Leu2198=
XM_017009329.1:c.6792A>G	XP_016864818.1:p.Leu2264=
XM_017009330.2:c.5175A>G	XP_016864819.1:p.Leu1725=
XM_017009331.1:c.5166A>G	XP_016864820.1:p.Leu1722=
NM_133433.4:c.6792A>G MANE Select	NP_597677.2:p.Leu2264=
NM_015384.5:c.6792A>G	NP_056199.2:p.Leu2264=