Canonical Allele Identifier: CA267557

Gene: NIPBL

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37049239C>G , CM000667.2:g.37049239C>G	GRCh38
NC_000005.9:g.37049341C>G , CM000667.1:g.37049341C>G	GRCh37
NC_000005.8:g.37085098C>G	NCBI36
NG_006987.1:g.177357C>G
NG_006987.2:g.177357C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.6892C>G MANE Select	ENSP00000282516.8:p.Arg2298Gly
ENST00000652901.1:c.6892C>G	ENSP00000499536.1:p.Arg2298Gly
ENST00000282516.12:c.6892C>G	ENSP00000282516.8:p.Arg2298Gly
ENST00000448238.2:c.6892C>G	ENSP00000406266.2:p.Arg2298Gly
ENST00000621733.1:c.1-15339C>G	ENSP00000480694.1:n.1-15339C>G
NM_015384.4:c.6892C>G	NP_056199.2:p.Arg2298Gly
NM_133433.3:c.6892C>G	NP_597677.2:p.Arg2298Gly
XM_005248280.2:c.6892C>G	XP_005248337.1:p.Arg2298Gly
XM_005248282.3:c.6148C>G	XP_005248339.2:p.Arg2050Gly
XM_006714467.2:c.6892C>G	XP_006714530.1:p.Arg2298Gly
XM_006714468.1:c.6694C>G	XP_006714531.1:p.Arg2232Gly
XM_011514014.1:c.6511C>G	XP_011512316.1:p.Arg2171Gly
XM_011514015.1:c.6892C>G	XP_011512317.1:p.Arg2298Gly
XM_005248280.3:c.6892C>G	XP_005248337.1:p.Arg2298Gly
XM_005248282.5:c.6232C>G	XP_005248339.3:p.Arg2078Gly
XM_006714468.2:c.6694C>G	XP_006714531.1:p.Arg2232Gly
XM_017009329.1:c.6892C>G	XP_016864818.1:p.Arg2298Gly
XM_017009330.2:c.5275C>G	XP_016864819.1:p.Arg1759Gly
XM_017009331.1:c.5266C>G	XP_016864820.1:p.Arg1756Gly
NM_133433.4:c.6892C>G MANE Select	NP_597677.2:p.Arg2298Gly
NM_015384.5:c.6892C>G	NP_056199.2:p.Arg2298Gly