Canonical Allele Identifier: CA117052570

Gene: NIPBL

Linked Data

• dbSNP Id: rs907389588
• MyVariant Identifiers: chr5:g.36995526A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36995526A>T , CM000667.2:g.36995526A>T	GRCh38
NC_000005.9:g.36995628A>T , CM000667.1:g.36995628A>T	GRCh37
NC_000005.8:g.37031385A>T	NCBI36
NG_006987.1:g.123644A>T
NG_006987.2:g.123644A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000282516.13:c.3122-96A>T MANE Select	ENSP00000282516.8:n.3122-96A>T
ENST00000652901.1:c.3122-96A>T	ENSP00000499536.1:n.3122-96A>T
ENST00000282516.12:c.3122-96A>T	ENSP00000282516.8:n.3122-96A>T
ENST00000448238.2:c.3122-96A>T	ENSP00000406266.2:n.3122-96A>T
ENST00000503274.1:n.377A>T
ENST00000504430.5:n.2742-96A>T
ENST00000621733.1:c.1-69052A>T	ENSP00000480694.1:n.1-69052A>T
NM_015384.4:c.3122-96A>T	NP_056199.2:n.3122-96A>T
NM_133433.3:c.3122-96A>T	NP_597677.2:n.3122-96A>T
XM_005248280.2:c.3122-96A>T	XP_005248337.1:n.3122-96A>T
XM_005248282.3:c.2378-96A>T	XP_005248339.2:n.2378-96A>T
XM_006714467.2:c.3122-96A>T	XP_006714530.1:n.3122-96A>T
XM_006714468.1:c.3122-96A>T	XP_006714531.1:n.3122-96A>T
XM_011514014.1:c.3122-5291A>T	XP_011512316.1:n.3122-5291A>T
XM_011514015.1:c.3122-96A>T	XP_011512317.1:n.3122-96A>T
XM_005248280.3:c.3122-96A>T	XP_005248337.1:n.3122-96A>T
XM_005248282.5:c.2462-96A>T	XP_005248339.3:n.2462-96A>T
XM_006714468.2:c.3122-96A>T	XP_006714531.1:n.3122-96A>T
XM_017009329.1:c.3122-96A>T	XP_016864818.1:n.3122-96A>T
XM_017009330.2:c.1505-96A>T	XP_016864819.1:n.1505-96A>T
XM_017009331.1:c.1496-96A>T	XP_016864820.1:n.1496-96A>T
NM_133433.4:c.3122-96A>T MANE Select	NP_597677.2:n.3122-96A>T
NM_015384.5:c.3122-96A>T	NP_056199.2:n.3122-96A>T