Canonical Allele Identifier: CA359506992

Gene: NIPBL

Linked Data

• dbSNP Id: rs1382410811
• gnomAD v2: 5-36986198-G-T
• gnomAD v3: 5-36986096-G-T
• gnomAD v4: 5-36986096-G-T
• MyVariant Identifiers: chr5:g.36986198G>T (hg19) ; chr5:g.36986096G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36986096G>T , CM000667.2:g.36986096G>T	GRCh38
NC_000005.9:g.36986198G>T , CM000667.1:g.36986198G>T	GRCh37
NC_000005.8:g.37021955G>T	NCBI36
NG_006987.1:g.114214G>T
NG_006987.2:g.114214G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.2916G>T MANE Select	ENSP00000282516.8:p.Glu972Asp
ENST00000652901.1:c.2916G>T	ENSP00000499536.1:p.Glu972Asp
ENST00000282516.12:c.2916G>T	ENSP00000282516.8:p.Glu972Asp
ENST00000448238.2:c.2916G>T	ENSP00000406266.2:p.Glu972Asp
ENST00000504430.5:n.2536G>T
ENST00000621733.1:c.1-78482G>T	ENSP00000480694.1:n.1-78482G>T
NM_015384.4:c.2916G>T	NP_056199.2:p.Glu972Asp
NM_133433.3:c.2916G>T	NP_597677.2:p.Glu972Asp
XM_005248280.2:c.2916G>T	XP_005248337.1:p.Glu972Asp
XM_005248282.3:c.2172G>T	XP_005248339.2:p.Glu724Asp
XM_006714467.2:c.2916G>T	XP_006714530.1:p.Glu972Asp
XM_006714468.1:c.2916G>T	XP_006714531.1:p.Glu972Asp
XM_011514014.1:c.2916G>T	XP_011512316.1:p.Glu972Asp
XM_011514015.1:c.2916G>T	XP_011512317.1:p.Glu972Asp
XM_005248280.3:c.2916G>T	XP_005248337.1:p.Glu972Asp
XM_005248282.5:c.2256G>T	XP_005248339.3:p.Glu752Asp
XM_006714468.2:c.2916G>T	XP_006714531.1:p.Glu972Asp
XM_017009329.1:c.2916G>T	XP_016864818.1:p.Glu972Asp
XM_017009330.2:c.1299G>T	XP_016864819.1:p.Glu433Asp
XM_017009331.1:c.1496-9526G>T	XP_016864820.1:n.1496-9526G>T
NM_133433.4:c.2916G>T MANE Select	NP_597677.2:p.Glu972Asp
NM_015384.5:c.2916G>T	NP_056199.2:p.Glu972Asp