Canonical Allele Identifier: CA1539579932
Gene: NIPBL HGNC NCBI

Linked Data

dbSNP Id: rs1744520388

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.36984559_36984564dup , CM000667.2:g.36984559_36984564dup GRCh38
NC_000005.9:g.36984661_36984666dup , CM000667.1:g.36984661_36984666dup GRCh37
NC_000005.8:g.37020418_37020423dup NCBI36
NG_006987.1:g.112677_112682dup
NG_006987.2:g.112677_112682dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000282516.13:c.1496-117_1496-112dup MANE Select ENSP00000282516.8:n.1496-117_1496-112dup
ENST00000652901.1:c.1496-117_1496-112dup ENSP00000499536.1:n.1496-117_1496-112dup
ENST00000282516.12:c.1496-117_1496-112dup ENSP00000282516.8:n.1496-117_1496-112dup
ENST00000448238.2:c.1496-117_1496-112dup ENSP00000406266.2:n.1496-117_1496-112dup
ENST00000504430.5:n.1116-117_1116-112dup
ENST00000621733.1:c.1-80019_1-80014dup ENSP00000480694.1:n.1-80019_1-80014dup
NM_015384.4:c.1496-117_1496-112dup NP_056199.2:n.1496-117_1496-112dup
NM_133433.3:c.1496-117_1496-112dup NP_597677.2:n.1496-117_1496-112dup
XM_005248280.2:c.1496-117_1496-112dup XP_005248337.1:n.1496-117_1496-112dup
XM_005248282.3:c.752-117_752-112dup XP_005248339.2:n.752-117_752-112dup
XM_006714467.2:c.1496-117_1496-112dup XP_006714530.1:n.1496-117_1496-112dup
XM_006714468.1:c.1496-117_1496-112dup XP_006714531.1:n.1496-117_1496-112dup
XM_011514014.1:c.1496-117_1496-112dup XP_011512316.1:n.1496-117_1496-112dup
XM_011514015.1:c.1496-117_1496-112dup XP_011512317.1:n.1496-117_1496-112dup
XM_005248280.3:c.1496-117_1496-112dup XP_005248337.1:n.1496-117_1496-112dup
XM_005248282.5:c.836-117_836-112dup XP_005248339.3:n.836-117_836-112dup
XM_006714468.2:c.1496-117_1496-112dup XP_006714531.1:n.1496-117_1496-112dup
XM_017009329.1:c.1496-117_1496-112dup XP_016864818.1:n.1496-117_1496-112dup
XM_017009330.2:c.-122-117_-122-112dup XP_016864819.1:n.-122-117_-122-112dup
XM_017009331.1:c.1495+8157_1495+8162dup XP_016864820.1:n.1495+8157_1495+8162dup
NM_133433.4:c.1496-117_1496-112dup MANE Select NP_597677.2:n.1496-117_1496-112dup
NM_015384.5:c.1496-117_1496-112dup NP_056199.2:n.1496-117_1496-112dup