Canonical Allele Identifier: CA359520194

Gene: NIPBL

Linked Data

• gnomAD v4: 5-37063844-G-T
• MyVariant Identifiers: chr5:g.37063946G>T (hg19) ; chr5:g.37063844G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37063844G>T , CM000667.2:g.37063844G>T	GRCh38
NC_000005.9:g.37063946G>T , CM000667.1:g.37063946G>T	GRCh37
NC_000005.8:g.37099703G>T	NCBI36
NG_006987.1:g.191962G>T
NG_006987.2:g.191962G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.7915G>T MANE Select	ENSP00000282516.8:p.Val2639Phe
ENST00000652901.1:c.7768G>T	ENSP00000499536.1:p.Val2590Phe
ENST00000282516.12:c.7915G>T	ENSP00000282516.8:p.Val2639Phe
ENST00000448238.2:c.7915G>T	ENSP00000406266.2:p.Val2639Phe
ENST00000513819.1:c.318G>T	ENSP00000421504.1:p.Arg106Ser
ENST00000514335.1:n.1797G>T
ENST00000621733.1:c.1-734G>T	ENSP00000480694.1:n.1-734G>T
NM_015384.4:c.7915G>T	NP_056199.2:p.Val2639Phe
NM_133433.3:c.7915G>T	NP_597677.2:p.Val2639Phe
XM_005248280.2:c.7915G>T	XP_005248337.1:p.Val2639Phe
XM_005248282.3:c.7171G>T	XP_005248339.2:p.Val2391Phe
XM_006714467.2:c.7768G>T	XP_006714530.1:p.Val2590Phe
XM_006714468.1:c.7717G>T	XP_006714531.1:p.Val2573Phe
XM_011514014.1:c.7534G>T	XP_011512316.1:p.Val2512Phe
XM_005248280.3:c.7915G>T	XP_005248337.1:p.Val2639Phe
XM_005248282.5:c.7255G>T	XP_005248339.3:p.Val2419Phe
XM_006714468.2:c.7717G>T	XP_006714531.1:p.Val2573Phe
XM_017009329.1:c.7768G>T	XP_016864818.1:p.Val2590Phe
XM_017009330.2:c.6298G>T	XP_016864819.1:p.Val2100Phe
XM_017009331.1:c.6289G>T	XP_016864820.1:p.Val2097Phe
NM_133433.4:c.7915G>T MANE Select	NP_597677.2:p.Val2639Phe
NM_015384.5:c.7915G>T	NP_056199.2:p.Val2639Phe