Canonical Allele Identifier: CA205205

Gene: NIPBL

Linked Data

• ClinVar Variation Id: 211641
• ClinVar RCV Id: RCV000192404
• dbSNP Id: rs797045765
• MyVariant Identifiers: chr5:g.37016276A>G (hg19) ; chr5:g.37016174A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37016174A>G , CM000667.2:g.37016174A>G	GRCh38
NC_000005.9:g.37016276A>G , CM000667.1:g.37016276A>G	GRCh37
NC_000005.8:g.37052033A>G	NCBI36
NG_006987.1:g.144292A>G
NG_006987.2:g.144292A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.4776+4A>G MANE Select	ENSP00000282516.8:n.4776+4A>G
ENST00000652901.1:c.4776+4A>G	ENSP00000499536.1:n.4776+4A>G
ENST00000282516.12:c.4776+4A>G	ENSP00000282516.8:n.4776+4A>G
ENST00000448238.2:c.4776+4A>G	ENSP00000406266.2:n.4776+4A>G
ENST00000621733.1:c.1-48404A>G	ENSP00000480694.1:n.1-48404A>G
NM_015384.4:c.4776+4A>G	NP_056199.2:n.4776+4A>G
NM_133433.3:c.4776+4A>G	NP_597677.2:n.4776+4A>G
XM_005248280.2:c.4776+4A>G	XP_005248337.1:n.4776+4A>G
XM_005248282.3:c.4032+4A>G	XP_005248339.2:n.4032+4A>G
XM_006714467.2:c.4776+4A>G	XP_006714530.1:n.4776+4A>G
XM_006714468.1:c.4578+4A>G	XP_006714531.1:n.4578+4A>G
XM_011514014.1:c.4395+4A>G	XP_011512316.1:n.4395+4A>G
XM_011514015.1:c.4776+4A>G	XP_011512317.1:n.4776+4A>G
XM_005248280.3:c.4776+4A>G	XP_005248337.1:n.4776+4A>G
XM_005248282.5:c.4116+4A>G	XP_005248339.3:n.4116+4A>G
XM_006714468.2:c.4578+4A>G	XP_006714531.1:n.4578+4A>G
XM_017009329.1:c.4776+4A>G	XP_016864818.1:n.4776+4A>G
XM_017009330.2:c.3159+4A>G	XP_016864819.1:n.3159+4A>G
XM_017009331.1:c.3150+4A>G	XP_016864820.1:n.3150+4A>G
NM_133433.4:c.4776+4A>G MANE Select	NP_597677.2:n.4776+4A>G
NM_015384.5:c.4776+4A>G	NP_056199.2:n.4776+4A>G