Canonical Allele Identifier: CA443910125

Gene: NIPBL

Linked Data

• MyVariant Identifiers: chr5:g.37051955G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37051853G>A , CM000667.2:g.37051853G>A	GRCh38
NC_000005.9:g.37051955G>A , CM000667.1:g.37051955G>A	GRCh37
NC_000005.8:g.37087712G>A	NCBI36
NG_006987.1:g.179971G>A
NG_006987.2:g.179971G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.7029G>A MANE Select	ENSP00000282516.8:p.Val2343=
ENST00000652901.1:c.7029G>A	ENSP00000499536.1:p.Val2343=
ENST00000282516.12:c.7029G>A	ENSP00000282516.8:p.Val2343=
ENST00000448238.2:c.7029G>A	ENSP00000406266.2:p.Val2343=
ENST00000514335.1:n.911G>A
ENST00000621733.1:c.1-12725G>A	ENSP00000480694.1:n.1-12725G>A
NM_015384.4:c.7029G>A	NP_056199.2:p.Val2343=
NM_133433.3:c.7029G>A	NP_597677.2:p.Val2343=
XM_005248280.2:c.7029G>A	XP_005248337.1:p.Val2343=
XM_005248282.3:c.6285G>A	XP_005248339.2:p.Val2095=
XM_006714467.2:c.7029G>A	XP_006714530.1:p.Val2343=
XM_006714468.1:c.6831G>A	XP_006714531.1:p.Val2277=
XM_011514014.1:c.6648G>A	XP_011512316.1:p.Val2216=
XM_011514015.1:c.7029G>A	XP_011512317.1:p.Val2343=
XM_005248280.3:c.7029G>A	XP_005248337.1:p.Val2343=
XM_005248282.5:c.6369G>A	XP_005248339.3:p.Val2123=
XM_006714468.2:c.6831G>A	XP_006714531.1:p.Val2277=
XM_017009329.1:c.7029G>A	XP_016864818.1:p.Val2343=
XM_017009330.2:c.5412G>A	XP_016864819.1:p.Val1804=
XM_017009331.1:c.5403G>A	XP_016864820.1:p.Val1801=
NM_133433.4:c.7029G>A MANE Select	NP_597677.2:p.Val2343=
NM_015384.5:c.7029G>A	NP_056199.2:p.Val2343=