Canonical Allele Identifier: CA359508796
Gene: NIPBL HGNC NCBI

Linked Data

gnomAD v4: 5-37049158-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37049158T>A , CM000667.2:g.37049158T>A GRCh38
NC_000005.9:g.37049260T>A , CM000667.1:g.37049260T>A GRCh37
NC_000005.8:g.37085017T>A NCBI36
NG_006987.1:g.177276T>A
NG_006987.2:g.177276T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282516.13:c.6811T>A MANE Select ENSP00000282516.8:p.Ser2271Thr
ENST00000652901.1:c.6811T>A ENSP00000499536.1:p.Ser2271Thr
ENST00000282516.12:c.6811T>A ENSP00000282516.8:p.Ser2271Thr
ENST00000448238.2:c.6811T>A ENSP00000406266.2:p.Ser2271Thr
ENST00000621733.1:c.1-15420T>A ENSP00000480694.1:n.1-15420T>A
NM_015384.4:c.6811T>A NP_056199.2:p.Ser2271Thr
NM_133433.3:c.6811T>A NP_597677.2:p.Ser2271Thr
XM_005248280.2:c.6811T>A XP_005248337.1:p.Ser2271Thr
XM_005248282.3:c.6067T>A XP_005248339.2:p.Ser2023Thr
XM_006714467.2:c.6811T>A XP_006714530.1:p.Ser2271Thr
XM_006714468.1:c.6613T>A XP_006714531.1:p.Ser2205Thr
XM_011514014.1:c.6430T>A XP_011512316.1:p.Ser2144Thr
XM_011514015.1:c.6811T>A XP_011512317.1:p.Ser2271Thr
XM_005248280.3:c.6811T>A XP_005248337.1:p.Ser2271Thr
XM_005248282.5:c.6151T>A XP_005248339.3:p.Ser2051Thr
XM_006714468.2:c.6613T>A XP_006714531.1:p.Ser2205Thr
XM_017009329.1:c.6811T>A XP_016864818.1:p.Ser2271Thr
XM_017009330.2:c.5194T>A XP_016864819.1:p.Ser1732Thr
XM_017009331.1:c.5185T>A XP_016864820.1:p.Ser1729Thr
NM_133433.4:c.6811T>A MANE Select NP_597677.2:p.Ser2271Thr
NM_015384.5:c.6811T>A NP_056199.2:p.Ser2271Thr