Canonical Allele Identifier: CA2673574279
Gene: NIPBL HGNC NCBI

Linked Data

gnomAD v4: 5-36995550-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.36995550G>A , CM000667.2:g.36995550G>A GRCh38
NC_000005.9:g.36995652G>A , CM000667.1:g.36995652G>A GRCh37
NC_000005.8:g.37031409G>A NCBI36
NG_006987.1:g.123668G>A
NG_006987.2:g.123668G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.3122-72G>A MANE Select ENSP00000282516.8:n.3122-72G>A
ENST00000652901.1:c.3122-72G>A ENSP00000499536.1:n.3122-72G>A
ENST00000282516.12:c.3122-72G>A ENSP00000282516.8:n.3122-72G>A
ENST00000448238.2:c.3122-72G>A ENSP00000406266.2:n.3122-72G>A
ENST00000503274.1:n.401G>A
ENST00000504430.5:n.2742-72G>A
ENST00000621733.1:c.1-69028G>A ENSP00000480694.1:n.1-69028G>A
NM_015384.4:c.3122-72G>A NP_056199.2:n.3122-72G>A
NM_133433.3:c.3122-72G>A NP_597677.2:n.3122-72G>A
XM_005248280.2:c.3122-72G>A XP_005248337.1:n.3122-72G>A
XM_005248282.3:c.2378-72G>A XP_005248339.2:n.2378-72G>A
XM_006714467.2:c.3122-72G>A XP_006714530.1:n.3122-72G>A
XM_006714468.1:c.3122-72G>A XP_006714531.1:n.3122-72G>A
XM_011514014.1:c.3122-5267G>A XP_011512316.1:n.3122-5267G>A
XM_011514015.1:c.3122-72G>A XP_011512317.1:n.3122-72G>A
XM_005248280.3:c.3122-72G>A XP_005248337.1:n.3122-72G>A
XM_005248282.5:c.2462-72G>A XP_005248339.3:n.2462-72G>A
XM_006714468.2:c.3122-72G>A XP_006714531.1:n.3122-72G>A
XM_017009329.1:c.3122-72G>A XP_016864818.1:n.3122-72G>A
XM_017009330.2:c.1505-72G>A XP_016864819.1:n.1505-72G>A
XM_017009331.1:c.1496-72G>A XP_016864820.1:n.1496-72G>A
NM_133433.4:c.3122-72G>A MANE Select NP_597677.2:n.3122-72G>A
NM_015384.5:c.3122-72G>A NP_056199.2:n.3122-72G>A