Canonical Allele Identifier: CA3236227

Gene: NIPBL

Linked Data

• dbSNP Id: rs769437048
• ExAC: 5:36986073 A / G
• gnomAD v3: 5-36985971-A-G
• gnomAD v4: 5-36985971-A-G
• MyVariant Identifiers: chr5:g.36986073A>G (hg19) ; chr5:g.36985971A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36985971A>G , CM000667.2:g.36985971A>G	GRCh38
NC_000005.9:g.36986073A>G , CM000667.1:g.36986073A>G	GRCh37
NC_000005.8:g.37021830A>G	NCBI36
NG_006987.1:g.114089A>G
NG_006987.2:g.114089A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000282516.13:c.2791A>G MANE Select	ENSP00000282516.8:p.Asn931Asp
ENST00000652901.1:c.2791A>G	ENSP00000499536.1:p.Asn931Asp
ENST00000282516.12:c.2791A>G	ENSP00000282516.8:p.Asn931Asp
ENST00000448238.2:c.2791A>G	ENSP00000406266.2:p.Asn931Asp
ENST00000504430.5:n.2411A>G
ENST00000621733.1:c.1-78607A>G	ENSP00000480694.1:n.1-78607A>G
NM_015384.4:c.2791A>G	NP_056199.2:p.Asn931Asp
NM_133433.3:c.2791A>G	NP_597677.2:p.Asn931Asp
XM_005248280.2:c.2791A>G	XP_005248337.1:p.Asn931Asp
XM_005248282.3:c.2047A>G	XP_005248339.2:p.Asn683Asp
XM_006714467.2:c.2791A>G	XP_006714530.1:p.Asn931Asp
XM_006714468.1:c.2791A>G	XP_006714531.1:p.Asn931Asp
XM_011514014.1:c.2791A>G	XP_011512316.1:p.Asn931Asp
XM_011514015.1:c.2791A>G	XP_011512317.1:p.Asn931Asp
XM_005248280.3:c.2791A>G	XP_005248337.1:p.Asn931Asp
XM_005248282.5:c.2131A>G	XP_005248339.3:p.Asn711Asp
XM_006714468.2:c.2791A>G	XP_006714531.1:p.Asn931Asp
XM_017009329.1:c.2791A>G	XP_016864818.1:p.Asn931Asp
XM_017009330.2:c.1174A>G	XP_016864819.1:p.Asn392Asp
XM_017009331.1:c.1495+9569A>G	XP_016864820.1:n.1495+9569A>G
NM_133433.4:c.2791A>G MANE Select	NP_597677.2:p.Asn931Asp
NM_015384.5:c.2791A>G	NP_056199.2:p.Asn931Asp