Canonical Allele Identifier: CA359509604

Gene: NIPBL

Linked Data

• MyVariant Identifiers: chr5:g.37051906G>T (hg19) ; chr5:g.37051804G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37051804G>T , CM000667.2:g.37051804G>T	GRCh38
NC_000005.9:g.37051906G>T , CM000667.1:g.37051906G>T	GRCh37
NC_000005.8:g.37087663G>T	NCBI36
NG_006987.1:g.179922G>T
NG_006987.2:g.179922G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.6980G>T MANE Select	ENSP00000282516.8:p.Gly2327Val
ENST00000652901.1:c.6980G>T	ENSP00000499536.1:p.Gly2327Val
ENST00000282516.12:c.6980G>T	ENSP00000282516.8:p.Gly2327Val
ENST00000448238.2:c.6980G>T	ENSP00000406266.2:p.Gly2327Val
ENST00000514335.1:n.862G>T
ENST00000621733.1:c.1-12774G>T	ENSP00000480694.1:n.1-12774G>T
NM_015384.4:c.6980G>T	NP_056199.2:p.Gly2327Val
NM_133433.3:c.6980G>T	NP_597677.2:p.Gly2327Val
XM_005248280.2:c.6980G>T	XP_005248337.1:p.Gly2327Val
XM_005248282.3:c.6236G>T	XP_005248339.2:p.Gly2079Val
XM_006714467.2:c.6980G>T	XP_006714530.1:p.Gly2327Val
XM_006714468.1:c.6782G>T	XP_006714531.1:p.Gly2261Val
XM_011514014.1:c.6599G>T	XP_011512316.1:p.Gly2200Val
XM_011514015.1:c.6980G>T	XP_011512317.1:p.Gly2327Val
XM_005248280.3:c.6980G>T	XP_005248337.1:p.Gly2327Val
XM_005248282.5:c.6320G>T	XP_005248339.3:p.Gly2107Val
XM_006714468.2:c.6782G>T	XP_006714531.1:p.Gly2261Val
XM_017009329.1:c.6980G>T	XP_016864818.1:p.Gly2327Val
XM_017009330.2:c.5363G>T	XP_016864819.1:p.Gly1788Val
XM_017009331.1:c.5354G>T	XP_016864820.1:p.Gly1785Val
NM_133433.4:c.6980G>T MANE Select	NP_597677.2:p.Gly2327Val
NM_015384.5:c.6980G>T	NP_056199.2:p.Gly2327Val