Canonical Allele Identifier: CA359500637

Gene: NIPBL

Linked Data

• dbSNP Id: rs1744670716
• gnomAD v3: 5-36985508-A-T
• gnomAD v4: 5-36985508-A-T
• MyVariant Identifiers: chr5:g.36985610A>T (hg19) ; chr5:g.36985508A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36985508A>T , CM000667.2:g.36985508A>T	GRCh38
NC_000005.9:g.36985610A>T , CM000667.1:g.36985610A>T	GRCh37
NC_000005.8:g.37021367A>T	NCBI36
NG_006987.1:g.113626A>T
NG_006987.2:g.113626A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.2328A>T MANE Select	ENSP00000282516.8:p.Lys776Asn
ENST00000652901.1:c.2328A>T	ENSP00000499536.1:p.Lys776Asn
ENST00000282516.12:c.2328A>T	ENSP00000282516.8:p.Lys776Asn
ENST00000448238.2:c.2328A>T	ENSP00000406266.2:p.Lys776Asn
ENST00000504430.5:n.1948A>T
ENST00000621733.1:c.1-79070A>T	ENSP00000480694.1:n.1-79070A>T
NM_015384.4:c.2328A>T	NP_056199.2:p.Lys776Asn
NM_133433.3:c.2328A>T	NP_597677.2:p.Lys776Asn
XM_005248280.2:c.2328A>T	XP_005248337.1:p.Lys776Asn
XM_005248282.3:c.1584A>T	XP_005248339.2:p.Lys528Asn
XM_006714467.2:c.2328A>T	XP_006714530.1:p.Lys776Asn
XM_006714468.1:c.2328A>T	XP_006714531.1:p.Lys776Asn
XM_011514014.1:c.2328A>T	XP_011512316.1:p.Lys776Asn
XM_011514015.1:c.2328A>T	XP_011512317.1:p.Lys776Asn
XM_005248280.3:c.2328A>T	XP_005248337.1:p.Lys776Asn
XM_005248282.5:c.1668A>T	XP_005248339.3:p.Lys556Asn
XM_006714468.2:c.2328A>T	XP_006714531.1:p.Lys776Asn
XM_017009329.1:c.2328A>T	XP_016864818.1:p.Lys776Asn
XM_017009330.2:c.711A>T	XP_016864819.1:p.Lys237Asn
XM_017009331.1:c.1495+9106A>T	XP_016864820.1:n.1495+9106A>T
NM_133433.4:c.2328A>T MANE Select	NP_597677.2:p.Lys776Asn
NM_015384.5:c.2328A>T	NP_056199.2:p.Lys776Asn