Canonical Allele Identifier: CA443905780

Gene: NIPBL

Linked Data

• dbSNP Id: rs1360819170
• gnomAD v2: 5-37038708-T-G
• gnomAD v4: 5-37038606-T-G
• MyVariant Identifiers: chr5:g.37038708T>G (hg19) ; chr5:g.37038606T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37038606T>G , CM000667.2:g.37038606T>G	GRCh38
NC_000005.9:g.37038708T>G , CM000667.1:g.37038708T>G	GRCh37
NC_000005.8:g.37074465T>G	NCBI36
NG_006987.1:g.166724T>G
NG_006987.2:g.166724T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.5976T>G MANE Select	ENSP00000282516.8:p.Ser1992=
ENST00000652901.1:c.5976T>G	ENSP00000499536.1:p.Ser1992=
ENST00000282516.12:c.5976T>G	ENSP00000282516.8:p.Ser1992=
ENST00000448238.2:c.5976T>G	ENSP00000406266.2:p.Ser1992=
ENST00000621733.1:c.1-25972T>G	ENSP00000480694.1:n.1-25972T>G
NM_015384.4:c.5976T>G	NP_056199.2:p.Ser1992=
NM_133433.3:c.5976T>G	NP_597677.2:p.Ser1992=
XM_005248280.2:c.5976T>G	XP_005248337.1:p.Ser1992=
XM_005248282.3:c.5232T>G	XP_005248339.2:p.Ser1744=
XM_006714467.2:c.5976T>G	XP_006714530.1:p.Ser1992=
XM_006714468.1:c.5778T>G	XP_006714531.1:p.Ser1926=
XM_011514014.1:c.5595T>G	XP_011512316.1:p.Ser1865=
XM_011514015.1:c.5976T>G	XP_011512317.1:p.Ser1992=
XM_005248280.3:c.5976T>G	XP_005248337.1:p.Ser1992=
XM_005248282.5:c.5316T>G	XP_005248339.3:p.Ser1772=
XM_006714468.2:c.5778T>G	XP_006714531.1:p.Ser1926=
XM_017009329.1:c.5976T>G	XP_016864818.1:p.Ser1992=
XM_017009330.2:c.4359T>G	XP_016864819.1:p.Ser1453=
XM_017009331.1:c.4350T>G	XP_016864820.1:p.Ser1450=
NM_133433.4:c.5976T>G MANE Select	NP_597677.2:p.Ser1992=
NM_015384.5:c.5976T>G	NP_056199.2:p.Ser1992=