Canonical Allele Identifier: CA10604161

Gene: NIPBL

Linked Data

• ClinVar Variation Id: 282380
• ClinVar RCV Id: RCV000324942
• dbSNP Id: rs886042385
• gnomAD v2: 5-36985453-C-T
• gnomAD v3: 5-36985351-C-T
• gnomAD v4: 5-36985351-C-T
• MyVariant Identifiers: chr5:g.36985453C>T (hg19) ; chr5:g.36985351C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36985351C>T , CM000667.2:g.36985351C>T	GRCh38
NC_000005.9:g.36985453C>T , CM000667.1:g.36985453C>T	GRCh37
NC_000005.8:g.37021210C>T	NCBI36
NG_006987.1:g.113469C>T
NG_006987.2:g.113469C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.2171C>T MANE Select	ENSP00000282516.8:p.Thr724Ile
ENST00000652901.1:c.2171C>T	ENSP00000499536.1:p.Thr724Ile
ENST00000282516.12:c.2171C>T	ENSP00000282516.8:p.Thr724Ile
ENST00000448238.2:c.2171C>T	ENSP00000406266.2:p.Thr724Ile
ENST00000504430.5:n.1791C>T
ENST00000621733.1:c.1-79227C>T	ENSP00000480694.1:n.1-79227C>T
NM_015384.4:c.2171C>T	NP_056199.2:p.Thr724Ile
NM_133433.3:c.2171C>T	NP_597677.2:p.Thr724Ile
XM_005248280.2:c.2171C>T	XP_005248337.1:p.Thr724Ile
XM_005248282.3:c.1427C>T	XP_005248339.2:p.Thr476Ile
XM_006714467.2:c.2171C>T	XP_006714530.1:p.Thr724Ile
XM_006714468.1:c.2171C>T	XP_006714531.1:p.Thr724Ile
XM_011514014.1:c.2171C>T	XP_011512316.1:p.Thr724Ile
XM_011514015.1:c.2171C>T	XP_011512317.1:p.Thr724Ile
XM_005248280.3:c.2171C>T	XP_005248337.1:p.Thr724Ile
XM_005248282.5:c.1511C>T	XP_005248339.3:p.Thr504Ile
XM_006714468.2:c.2171C>T	XP_006714531.1:p.Thr724Ile
XM_017009329.1:c.2171C>T	XP_016864818.1:p.Thr724Ile
XM_017009330.2:c.554C>T	XP_016864819.1:p.Thr185Ile
XM_017009331.1:c.1495+8949C>T	XP_016864820.1:n.1495+8949C>T
NM_133433.4:c.2171C>T MANE Select	NP_597677.2:p.Thr724Ile
NM_015384.5:c.2171C>T	NP_056199.2:p.Thr724Ile