Canonical Allele Identifier: CA359518426

Gene: NIPBL

Linked Data

• MyVariant Identifiers: chr5:g.37060984T>G (hg19) ; chr5:g.37060882T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37060882T>G , CM000667.2:g.37060882T>G	GRCh38
NC_000005.9:g.37060984T>G , CM000667.1:g.37060984T>G	GRCh37
NC_000005.8:g.37096741T>G	NCBI36
NG_006987.1:g.189000T>G
NG_006987.2:g.189000T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000282516.13:c.7724T>G MANE Select	ENSP00000282516.8:p.Val2575Gly
ENST00000652901.1:c.7577T>G	ENSP00000499536.1:p.Val2526Gly
ENST00000282516.12:c.7724T>G	ENSP00000282516.8:p.Val2575Gly
ENST00000448238.2:c.7724T>G	ENSP00000406266.2:p.Val2575Gly
ENST00000513819.1:c.263+1717T>G	ENSP00000421504.1:n.263+1717T>G
ENST00000514335.1:n.1606T>G
ENST00000621733.1:c.1-3696T>G	ENSP00000480694.1:n.1-3696T>G
NM_015384.4:c.7724T>G	NP_056199.2:p.Val2575Gly
NM_133433.3:c.7724T>G	NP_597677.2:p.Val2575Gly
XM_005248280.2:c.7724T>G	XP_005248337.1:p.Val2575Gly
XM_005248282.3:c.6980T>G	XP_005248339.2:p.Val2327Gly
XM_006714467.2:c.7577T>G	XP_006714530.1:p.Val2526Gly
XM_006714468.1:c.7526T>G	XP_006714531.1:p.Val2509Gly
XM_011514014.1:c.7343T>G	XP_011512316.1:p.Val2448Gly
XM_011514015.1:c.*36T>G	XP_011512317.1:n.*36T>G
XM_005248280.3:c.7724T>G	XP_005248337.1:p.Val2575Gly
XM_005248282.5:c.7064T>G	XP_005248339.3:p.Val2355Gly
XM_006714468.2:c.7526T>G	XP_006714531.1:p.Val2509Gly
XM_017009329.1:c.7577T>G	XP_016864818.1:p.Val2526Gly
XM_017009330.2:c.6107T>G	XP_016864819.1:p.Val2036Gly
XM_017009331.1:c.6098T>G	XP_016864820.1:p.Val2033Gly
NM_133433.4:c.7724T>G MANE Select	NP_597677.2:p.Val2575Gly
NM_015384.5:c.7724T>G	NP_056199.2:p.Val2575Gly