Canonical Allele Identifier: CA359488362

Gene: NIPBL

Linked Data

• MyVariant Identifiers: chr5:g.37020955G>C (hg19) ; chr5:g.37020853G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37020853G>C , CM000667.2:g.37020853G>C	GRCh38
NC_000005.9:g.37020955G>C , CM000667.1:g.37020955G>C	GRCh37
NC_000005.8:g.37056712G>C	NCBI36
NG_006987.1:g.148971G>C
NG_006987.2:g.148971G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.5304G>C MANE Select	ENSP00000282516.8:p.Gln1768His
ENST00000652901.1:c.5304G>C	ENSP00000499536.1:p.Gln1768His
ENST00000282516.12:c.5304G>C	ENSP00000282516.8:p.Gln1768His
ENST00000448238.2:c.5304G>C	ENSP00000406266.2:p.Gln1768His
ENST00000621733.1:c.1-43725G>C	ENSP00000480694.1:n.1-43725G>C
NM_015384.4:c.5304G>C	NP_056199.2:p.Gln1768His
NM_133433.3:c.5304G>C	NP_597677.2:p.Gln1768His
XM_005248280.2:c.5304G>C	XP_005248337.1:p.Gln1768His
XM_005248282.3:c.4560G>C	XP_005248339.2:p.Gln1520His
XM_006714467.2:c.5304G>C	XP_006714530.1:p.Gln1768His
XM_006714468.1:c.5106G>C	XP_006714531.1:p.Gln1702His
XM_011514014.1:c.4923G>C	XP_011512316.1:p.Gln1641His
XM_011514015.1:c.5304G>C	XP_011512317.1:p.Gln1768His
XM_005248280.3:c.5304G>C	XP_005248337.1:p.Gln1768His
XM_005248282.5:c.4644G>C	XP_005248339.3:p.Gln1548His
XM_006714468.2:c.5106G>C	XP_006714531.1:p.Gln1702His
XM_017009329.1:c.5304G>C	XP_016864818.1:p.Gln1768His
XM_017009330.2:c.3687G>C	XP_016864819.1:p.Gln1229His
XM_017009331.1:c.3678G>C	XP_016864820.1:p.Gln1226His
NM_133433.4:c.5304G>C MANE Select	NP_597677.2:p.Gln1768His
NM_015384.5:c.5304G>C	NP_056199.2:p.Gln1768His