Canonical Allele Identifier: CA3236378
Gene: NIPBL HGNC NCBI

Linked Data

dbSNP Id: rs771636150
gnomAD v2: 5-37001046-C-T
gnomAD v4: 5-37000944-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37000944C>T , CM000667.2:g.37000944C>T GRCh38
NC_000005.9:g.37001046C>T , CM000667.1:g.37001046C>T GRCh37
NC_000005.8:g.37036803C>T NCBI36
NG_006987.1:g.129062C>T
NG_006987.2:g.129062C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.3575-45C>T MANE Select ENSP00000282516.8:n.3575-45C>T
ENST00000652901.1:c.3575-45C>T ENSP00000499536.1:n.3575-45C>T
ENST00000282516.12:c.3575-45C>T ENSP00000282516.8:n.3575-45C>T
ENST00000448238.2:c.3575-45C>T ENSP00000406266.2:n.3575-45C>T
ENST00000621733.1:c.1-63634C>T ENSP00000480694.1:n.1-63634C>T
NM_015384.4:c.3575-45C>T NP_056199.2:n.3575-45C>T
NM_133433.3:c.3575-45C>T NP_597677.2:n.3575-45C>T
XM_005248280.2:c.3575-45C>T XP_005248337.1:n.3575-45C>T
XM_005248282.3:c.2831-45C>T XP_005248339.2:n.2831-45C>T
XM_006714467.2:c.3575-45C>T XP_006714530.1:n.3575-45C>T
XM_006714468.1:c.3377-45C>T XP_006714531.1:n.3377-45C>T
XM_011514014.1:c.3194-45C>T XP_011512316.1:n.3194-45C>T
XM_011514015.1:c.3575-45C>T XP_011512317.1:n.3575-45C>T
XM_005248280.3:c.3575-45C>T XP_005248337.1:n.3575-45C>T
XM_005248282.5:c.2915-45C>T XP_005248339.3:n.2915-45C>T
XM_006714468.2:c.3377-45C>T XP_006714531.1:n.3377-45C>T
XM_017009329.1:c.3575-45C>T XP_016864818.1:n.3575-45C>T
XM_017009330.2:c.1958-45C>T XP_016864819.1:n.1958-45C>T
XM_017009331.1:c.1949-45C>T XP_016864820.1:n.1949-45C>T
NM_133433.4:c.3575-45C>T MANE Select NP_597677.2:n.3575-45C>T
NM_015384.5:c.3575-45C>T NP_056199.2:n.3575-45C>T