Canonical Allele Identifier: CA359520237
Gene: NIPBL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37063855C>G , CM000667.2:g.37063855C>G GRCh38
NC_000005.9:g.37063957C>G , CM000667.1:g.37063957C>G GRCh37
NC_000005.8:g.37099714C>G NCBI36
NG_006987.1:g.191973C>G
NG_006987.2:g.191973C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282516.13:c.7926C>G MANE Select ENSP00000282516.8:p.Ser2642Arg
ENST00000652901.1:c.7779C>G ENSP00000499536.1:p.Ser2593Arg
ENST00000282516.12:c.7926C>G ENSP00000282516.8:p.Ser2642Arg
ENST00000448238.2:c.7926C>G ENSP00000406266.2:p.Ser2642Arg
ENST00000513819.1:c.329C>G ENSP00000421504.1:p.Ala110Gly
ENST00000514335.1:n.1808C>G
ENST00000621733.1:c.1-723C>G ENSP00000480694.1:n.1-723C>G
NM_015384.4:c.7926C>G NP_056199.2:p.Ser2642Arg
NM_133433.3:c.7926C>G NP_597677.2:p.Ser2642Arg
XM_005248280.2:c.7926C>G XP_005248337.1:p.Ser2642Arg
XM_005248282.3:c.7182C>G XP_005248339.2:p.Ser2394Arg
XM_006714467.2:c.7779C>G XP_006714530.1:p.Ser2593Arg
XM_006714468.1:c.7728C>G XP_006714531.1:p.Ser2576Arg
XM_011514014.1:c.7545C>G XP_011512316.1:p.Ser2515Arg
XM_005248280.3:c.7926C>G XP_005248337.1:p.Ser2642Arg
XM_005248282.5:c.7266C>G XP_005248339.3:p.Ser2422Arg
XM_006714468.2:c.7728C>G XP_006714531.1:p.Ser2576Arg
XM_017009329.1:c.7779C>G XP_016864818.1:p.Ser2593Arg
XM_017009330.2:c.6309C>G XP_016864819.1:p.Ser2103Arg
XM_017009331.1:c.6300C>G XP_016864820.1:p.Ser2100Arg
NM_133433.4:c.7926C>G MANE Select NP_597677.2:p.Ser2642Arg
NM_015384.5:c.7926C>G NP_056199.2:p.Ser2642Arg