Canonical Allele Identifier: CA117036939

Gene: NIPBL

Linked Data

• dbSNP Id: rs200548405
• gnomAD v3: 5-37036447-C-T
• gnomAD v4: 5-37036447-C-T
• MyVariant Identifiers: chr5:g.37036549C>T (hg19) ; chr5:g.37036447C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37036447C>T , CM000667.2:g.37036447C>T	GRCh38
NC_000005.9:g.37036549C>T , CM000667.1:g.37036549C>T	GRCh37
NC_000005.8:g.37072306C>T	NCBI36
NG_006987.1:g.164565C>T
NG_006987.2:g.164565C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.5931C>T MANE Select	ENSP00000282516.8:p.Asn1977=
ENST00000652901.1:c.5931C>T	ENSP00000499536.1:p.Asn1977=
ENST00000282516.12:c.5931C>T	ENSP00000282516.8:p.Asn1977=
ENST00000448238.2:c.5931C>T	ENSP00000406266.2:p.Asn1977=
ENST00000621733.1:c.1-28131C>T	ENSP00000480694.1:n.1-28131C>T
NM_015384.4:c.5931C>T	NP_056199.2:p.Asn1977=
NM_133433.3:c.5931C>T	NP_597677.2:p.Asn1977=
XM_005248280.2:c.5931C>T	XP_005248337.1:p.Asn1977=
XM_005248282.3:c.5187C>T	XP_005248339.2:p.Asn1729=
XM_006714467.2:c.5931C>T	XP_006714530.1:p.Asn1977=
XM_006714468.1:c.5733C>T	XP_006714531.1:p.Asn1911=
XM_011514014.1:c.5550C>T	XP_011512316.1:p.Asn1850=
XM_011514015.1:c.5931C>T	XP_011512317.1:p.Asn1977=
XM_005248280.3:c.5931C>T	XP_005248337.1:p.Asn1977=
XM_005248282.5:c.5271C>T	XP_005248339.3:p.Asn1757=
XM_006714468.2:c.5733C>T	XP_006714531.1:p.Asn1911=
XM_017009329.1:c.5931C>T	XP_016864818.1:p.Asn1977=
XM_017009330.2:c.4314C>T	XP_016864819.1:p.Asn1438=
XM_017009331.1:c.4305C>T	XP_016864820.1:p.Asn1435=
NM_133433.4:c.5931C>T MANE Select	NP_597677.2:p.Asn1977=
NM_015384.5:c.5931C>T	NP_056199.2:p.Asn1977=