Canonical Allele Identifier: CA359514471

Gene: NIPBL

Linked Data

• MyVariant Identifiers: chr5:g.36995901T>G (hg19) ; chr5:g.36995799T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36995799T>G , CM000667.2:g.36995799T>G	GRCh38
NC_000005.9:g.36995901T>G , CM000667.1:g.36995901T>G	GRCh37
NC_000005.8:g.37031658T>G	NCBI36
NG_006987.1:g.123917T>G
NG_006987.2:g.123917T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.3299T>G MANE Select	ENSP00000282516.8:p.Phe1100Cys
ENST00000652901.1:c.3299T>G	ENSP00000499536.1:p.Phe1100Cys
ENST00000282516.12:c.3299T>G	ENSP00000282516.8:p.Phe1100Cys
ENST00000448238.2:c.3299T>G	ENSP00000406266.2:p.Phe1100Cys
ENST00000503274.1:n.650T>G
ENST00000504430.5:n.2919T>G
ENST00000509429.1:n.50T>G
ENST00000621733.1:c.1-68779T>G	ENSP00000480694.1:n.1-68779T>G
NM_015384.4:c.3299T>G	NP_056199.2:p.Phe1100Cys
NM_133433.3:c.3299T>G	NP_597677.2:p.Phe1100Cys
XM_005248280.2:c.3299T>G	XP_005248337.1:p.Phe1100Cys
XM_005248282.3:c.2555T>G	XP_005248339.2:p.Phe852Cys
XM_006714467.2:c.3299T>G	XP_006714530.1:p.Phe1100Cys
XM_006714468.1:c.3299T>G	XP_006714531.1:p.Phe1100Cys
XM_011514014.1:c.3122-5018T>G	XP_011512316.1:n.3122-5018T>G
XM_011514015.1:c.3299T>G	XP_011512317.1:p.Phe1100Cys
XM_005248280.3:c.3299T>G	XP_005248337.1:p.Phe1100Cys
XM_005248282.5:c.2639T>G	XP_005248339.3:p.Phe880Cys
XM_006714468.2:c.3299T>G	XP_006714531.1:p.Phe1100Cys
XM_017009329.1:c.3299T>G	XP_016864818.1:p.Phe1100Cys
XM_017009330.2:c.1682T>G	XP_016864819.1:p.Phe561Cys
XM_017009331.1:c.1673T>G	XP_016864820.1:p.Phe558Cys
NM_133433.4:c.3299T>G MANE Select	NP_597677.2:p.Phe1100Cys
NM_015384.5:c.3299T>G	NP_056199.2:p.Phe1100Cys