Canonical Allele Identifier: CA810303649

Gene: NIPBL

Linked Data

• dbSNP Id: rs1403516312
• gnomAD v3: 5-37045625-T-A
• gnomAD v4: 5-37045625-T-A
• MyVariant Identifiers: chr5:g.37045727T>A (hg19) ; chr5:g.37045625T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37045625T>A , CM000667.2:g.37045625T>A	GRCh38
NC_000005.9:g.37045727T>A , CM000667.1:g.37045727T>A	GRCh37
NC_000005.8:g.37081484T>A	NCBI36
NG_006987.1:g.173743T>A
NG_006987.2:g.173743T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.6498+28T>A MANE Select	ENSP00000282516.8:n.6498+28T>A
ENST00000652901.1:c.6498+28T>A	ENSP00000499536.1:n.6498+28T>A
ENST00000282516.12:c.6498+28T>A	ENSP00000282516.8:n.6498+28T>A
ENST00000448238.2:c.6498+28T>A	ENSP00000406266.2:n.6498+28T>A
ENST00000621733.1:c.1-18953T>A	ENSP00000480694.1:n.1-18953T>A
NM_015384.4:c.6498+28T>A	NP_056199.2:n.6498+28T>A
NM_133433.3:c.6498+28T>A	NP_597677.2:n.6498+28T>A
XM_005248280.2:c.6498+28T>A	XP_005248337.1:n.6498+28T>A
XM_005248282.3:c.5754+28T>A	XP_005248339.2:n.5754+28T>A
XM_006714467.2:c.6498+28T>A	XP_006714530.1:n.6498+28T>A
XM_006714468.1:c.6300+28T>A	XP_006714531.1:n.6300+28T>A
XM_011514014.1:c.6117+28T>A	XP_011512316.1:n.6117+28T>A
XM_011514015.1:c.6498+28T>A	XP_011512317.1:n.6498+28T>A
XM_005248280.3:c.6498+28T>A	XP_005248337.1:n.6498+28T>A
XM_005248282.5:c.5838+28T>A	XP_005248339.3:n.5838+28T>A
XM_006714468.2:c.6300+28T>A	XP_006714531.1:n.6300+28T>A
XM_017009329.1:c.6498+28T>A	XP_016864818.1:n.6498+28T>A
XM_017009330.2:c.4881+28T>A	XP_016864819.1:n.4881+28T>A
XM_017009331.1:c.4872+28T>A	XP_016864820.1:n.4872+28T>A
NM_133433.4:c.6498+28T>A MANE Select	NP_597677.2:n.6498+28T>A
NM_015384.5:c.6498+28T>A	NP_056199.2:n.6498+28T>A