Canonical Allele Identifier: CA443903937

Gene: NIPBL

Linked Data

• gnomAD v4: 5-36995734-A-T
• MyVariant Identifiers: chr5:g.36995836A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36995734A>T , CM000667.2:g.36995734A>T	GRCh38
NC_000005.9:g.36995836A>T , CM000667.1:g.36995836A>T	GRCh37
NC_000005.8:g.37031593A>T	NCBI36
NG_006987.1:g.123852A>T
NG_006987.2:g.123852A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.3234A>T MANE Select	ENSP00000282516.8:p.Thr1078=
ENST00000652901.1:c.3234A>T	ENSP00000499536.1:p.Thr1078=
ENST00000282516.12:c.3234A>T	ENSP00000282516.8:p.Thr1078=
ENST00000448238.2:c.3234A>T	ENSP00000406266.2:p.Thr1078=
ENST00000503274.1:n.585A>T
ENST00000504430.5:n.2854A>T
ENST00000621733.1:c.1-68844A>T	ENSP00000480694.1:n.1-68844A>T
NM_015384.4:c.3234A>T	NP_056199.2:p.Thr1078=
NM_133433.3:c.3234A>T	NP_597677.2:p.Thr1078=
XM_005248280.2:c.3234A>T	XP_005248337.1:p.Thr1078=
XM_005248282.3:c.2490A>T	XP_005248339.2:p.Thr830=
XM_006714467.2:c.3234A>T	XP_006714530.1:p.Thr1078=
XM_006714468.1:c.3234A>T	XP_006714531.1:p.Thr1078=
XM_011514014.1:c.3122-5083A>T	XP_011512316.1:n.3122-5083A>T
XM_011514015.1:c.3234A>T	XP_011512317.1:p.Thr1078=
XM_005248280.3:c.3234A>T	XP_005248337.1:p.Thr1078=
XM_005248282.5:c.2574A>T	XP_005248339.3:p.Thr858=
XM_006714468.2:c.3234A>T	XP_006714531.1:p.Thr1078=
XM_017009329.1:c.3234A>T	XP_016864818.1:p.Thr1078=
XM_017009330.2:c.1617A>T	XP_016864819.1:p.Thr539=
XM_017009331.1:c.1608A>T	XP_016864820.1:p.Thr536=
NM_133433.4:c.3234A>T MANE Select	NP_597677.2:p.Thr1078=
NM_015384.5:c.3234A>T	NP_056199.2:p.Thr1078=