Canonical Allele Identifier: CA359494304

Gene: NIPBL

Linked Data

• gnomAD v4: 5-36984900-A-G
• MyVariant Identifiers: chr5:g.36985002A>G (hg19) ; chr5:g.36984900A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36984900A>G , CM000667.2:g.36984900A>G	GRCh38
NC_000005.9:g.36985002A>G , CM000667.1:g.36985002A>G	GRCh37
NC_000005.8:g.37020759A>G	NCBI36
NG_006987.1:g.113018A>G
NG_006987.2:g.113018A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000282516.13:c.1720A>G MANE Select	ENSP00000282516.8:p.Asn574Asp
ENST00000652901.1:c.1720A>G	ENSP00000499536.1:p.Asn574Asp
ENST00000282516.12:c.1720A>G	ENSP00000282516.8:p.Asn574Asp
ENST00000448238.2:c.1720A>G	ENSP00000406266.2:p.Asn574Asp
ENST00000504430.5:n.1340A>G
ENST00000621733.1:c.1-79678A>G	ENSP00000480694.1:n.1-79678A>G
NM_015384.4:c.1720A>G	NP_056199.2:p.Asn574Asp
NM_133433.3:c.1720A>G	NP_597677.2:p.Asn574Asp
XM_005248280.2:c.1720A>G	XP_005248337.1:p.Asn574Asp
XM_005248282.3:c.976A>G	XP_005248339.2:p.Asn326Asp
XM_006714467.2:c.1720A>G	XP_006714530.1:p.Asn574Asp
XM_006714468.1:c.1720A>G	XP_006714531.1:p.Asn574Asp
XM_011514014.1:c.1720A>G	XP_011512316.1:p.Asn574Asp
XM_011514015.1:c.1720A>G	XP_011512317.1:p.Asn574Asp
XM_005248280.3:c.1720A>G	XP_005248337.1:p.Asn574Asp
XM_005248282.5:c.1060A>G	XP_005248339.3:p.Asn354Asp
XM_006714468.2:c.1720A>G	XP_006714531.1:p.Asn574Asp
XM_017009329.1:c.1720A>G	XP_016864818.1:p.Asn574Asp
XM_017009330.2:c.103A>G	XP_016864819.1:p.Asn35Asp
XM_017009331.1:c.1495+8498A>G	XP_016864820.1:n.1495+8498A>G
NM_133433.4:c.1720A>G MANE Select	NP_597677.2:p.Asn574Asp
NM_015384.5:c.1720A>G	NP_056199.2:p.Asn574Asp