Canonical Allele Identifier: CA359513241
Gene: NIPBL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.36995620A>T , CM000667.2:g.36995620A>T GRCh38
NC_000005.9:g.36995722A>T , CM000667.1:g.36995722A>T GRCh37
NC_000005.8:g.37031479A>T NCBI36
NG_006987.1:g.123738A>T
NG_006987.2:g.123738A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.3122-2A>T MANE Select ENSP00000282516.8:n.3122-2A>T
ENST00000652901.1:c.3122-2A>T ENSP00000499536.1:n.3122-2A>T
ENST00000282516.12:c.3122-2A>T ENSP00000282516.8:n.3122-2A>T
ENST00000448238.2:c.3122-2A>T ENSP00000406266.2:n.3122-2A>T
ENST00000503274.1:n.471A>T
ENST00000504430.5:n.2742-2A>T
ENST00000621733.1:c.1-68958A>T ENSP00000480694.1:n.1-68958A>T
NM_015384.4:c.3122-2A>T NP_056199.2:n.3122-2A>T
NM_133433.3:c.3122-2A>T NP_597677.2:n.3122-2A>T
XM_005248280.2:c.3122-2A>T XP_005248337.1:n.3122-2A>T
XM_005248282.3:c.2378-2A>T XP_005248339.2:n.2378-2A>T
XM_006714467.2:c.3122-2A>T XP_006714530.1:n.3122-2A>T
XM_006714468.1:c.3122-2A>T XP_006714531.1:n.3122-2A>T
XM_011514014.1:c.3122-5197A>T XP_011512316.1:n.3122-5197A>T
XM_011514015.1:c.3122-2A>T XP_011512317.1:n.3122-2A>T
XM_005248280.3:c.3122-2A>T XP_005248337.1:n.3122-2A>T
XM_005248282.5:c.2462-2A>T XP_005248339.3:n.2462-2A>T
XM_006714468.2:c.3122-2A>T XP_006714531.1:n.3122-2A>T
XM_017009329.1:c.3122-2A>T XP_016864818.1:n.3122-2A>T
XM_017009330.2:c.1505-2A>T XP_016864819.1:n.1505-2A>T
XM_017009331.1:c.1496-2A>T XP_016864820.1:n.1496-2A>T
NM_133433.4:c.3122-2A>T MANE Select NP_597677.2:n.3122-2A>T
NM_015384.5:c.3122-2A>T NP_056199.2:n.3122-2A>T