Canonical Allele Identifier: CA359514005

Gene: NIPBL

Linked Data

• MyVariant Identifiers: chr5:g.36995865T>C (hg19) ; chr5:g.36995763T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36995763T>C , CM000667.2:g.36995763T>C	GRCh38
NC_000005.9:g.36995865T>C , CM000667.1:g.36995865T>C	GRCh37
NC_000005.8:g.37031622T>C	NCBI36
NG_006987.1:g.123881T>C
NG_006987.2:g.123881T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.3263T>C MANE Select	ENSP00000282516.8:p.Ile1088Thr
ENST00000652901.1:c.3263T>C	ENSP00000499536.1:p.Ile1088Thr
ENST00000282516.12:c.3263T>C	ENSP00000282516.8:p.Ile1088Thr
ENST00000448238.2:c.3263T>C	ENSP00000406266.2:p.Ile1088Thr
ENST00000503274.1:n.614T>C
ENST00000504430.5:n.2883T>C
ENST00000509429.1:n.14T>C
ENST00000621733.1:c.1-68815T>C	ENSP00000480694.1:n.1-68815T>C
NM_015384.4:c.3263T>C	NP_056199.2:p.Ile1088Thr
NM_133433.3:c.3263T>C	NP_597677.2:p.Ile1088Thr
XM_005248280.2:c.3263T>C	XP_005248337.1:p.Ile1088Thr
XM_005248282.3:c.2519T>C	XP_005248339.2:p.Ile840Thr
XM_006714467.2:c.3263T>C	XP_006714530.1:p.Ile1088Thr
XM_006714468.1:c.3263T>C	XP_006714531.1:p.Ile1088Thr
XM_011514014.1:c.3122-5054T>C	XP_011512316.1:n.3122-5054T>C
XM_011514015.1:c.3263T>C	XP_011512317.1:p.Ile1088Thr
XM_005248280.3:c.3263T>C	XP_005248337.1:p.Ile1088Thr
XM_005248282.5:c.2603T>C	XP_005248339.3:p.Ile868Thr
XM_006714468.2:c.3263T>C	XP_006714531.1:p.Ile1088Thr
XM_017009329.1:c.3263T>C	XP_016864818.1:p.Ile1088Thr
XM_017009330.2:c.1646T>C	XP_016864819.1:p.Ile549Thr
XM_017009331.1:c.1637T>C	XP_016864820.1:p.Ile546Thr
NM_133433.4:c.3263T>C MANE Select	NP_597677.2:p.Ile1088Thr
NM_015384.5:c.3263T>C	NP_056199.2:p.Ile1088Thr