Canonical Allele Identifier: CA359486421
Gene: NIPBL HGNC NCBI

Linked Data

gnomAD v4: 5-36976207-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.36976207G>A , CM000667.2:g.36976207G>A GRCh38
NC_000005.9:g.36976309G>A , CM000667.1:g.36976309G>A GRCh37
NC_000005.8:g.37012066G>A NCBI36
NG_006987.1:g.104325G>A
NG_006987.2:g.104325G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000282516.13:c.1300G>A MANE Select ENSP00000282516.8:p.Val434Met
ENST00000652901.1:c.1300G>A ENSP00000499536.1:p.Val434Met
ENST00000282516.12:c.1300G>A ENSP00000282516.8:p.Val434Met
ENST00000448238.2:c.1300G>A ENSP00000406266.2:p.Val434Met
ENST00000504430.5:n.920G>A
ENST00000621733.1:c.1-88371G>A ENSP00000480694.1:n.1-88371G>A
NM_015384.4:c.1300G>A NP_056199.2:p.Val434Met
NM_133433.3:c.1300G>A NP_597677.2:p.Val434Met
XM_005248280.2:c.1300G>A XP_005248337.1:p.Val434Met
XM_005248282.3:c.556G>A XP_005248339.2:p.Val186Met
XM_006714467.2:c.1300G>A XP_006714530.1:p.Val434Met
XM_006714468.1:c.1300G>A XP_006714531.1:p.Val434Met
XM_011514014.1:c.1300G>A XP_011512316.1:p.Val434Met
XM_011514015.1:c.1300G>A XP_011512317.1:p.Val434Met
XM_005248280.3:c.1300G>A XP_005248337.1:p.Val434Met
XM_005248282.5:c.640G>A XP_005248339.3:p.Val214Met
XM_006714468.2:c.1300G>A XP_006714531.1:p.Val434Met
XM_017009329.1:c.1300G>A XP_016864818.1:p.Val434Met
XM_017009331.1:c.1300G>A XP_016864820.1:p.Val434Met
NM_133433.4:c.1300G>A MANE Select NP_597677.2:p.Val434Met
NM_015384.5:c.1300G>A NP_056199.2:p.Val434Met