Canonical Allele Identifier: CA444096536

Gene: NIPBL CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37064826T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37064724T>A , CM000667.2:g.37064724T>A	GRCh38
NC_000005.9:g.37064826T>A , CM000667.1:g.37064826T>A	GRCh37
NC_000005.8:g.37100583T>A	NCBI36
NG_006987.1:g.192842T>A
NG_006987.2:g.192842T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.8247T>A (NIPBL) MANE Select	ENSP00000282516.8:p.Thr2749=
ENST00000652901.1:c.*191T>A (NIPBL)	ENSP00000499536.1:n.*191T>A
ENST00000282516.12:c.8247T>A (NIPBL)	ENSP00000282516.8:p.Thr2749=
ENST00000514335.1:n.2170T>A (NIPBL)
ENST00000621733.1:c.147T>A (NIPBL)	ENSP00000480694.1:p.Thr49=
NM_015384.4:c.*701T>A (NIPBL)	NP_056199.2:n.*701T>A
NM_133433.3:c.8247T>A (NIPBL)	NP_597677.2:p.Thr2749=
XM_005248280.2:c.*191T>A (NIPBL)	XP_005248337.1:n.*191T>A
XM_005248282.3:c.7503T>A (NIPBL)	XP_005248339.2:p.Thr2501=
XM_006714467.2:c.8100T>A (NIPBL)	XP_006714530.1:p.Thr2700=
XM_006714468.1:c.8049T>A (NIPBL)	XP_006714531.1:p.Thr2683=
XM_011514014.1:c.7866T>A (NIPBL)	XP_011512316.1:p.Thr2622=
XM_005248280.3:c.*191T>A (NIPBL)	XP_005248337.1:n.*191T>A
XM_005248282.5:c.7587T>A (NIPBL)	XP_005248339.3:p.Thr2529=
XM_006714468.2:c.8049T>A (NIPBL)	XP_006714531.1:p.Thr2683=
XM_017009329.1:c.*191T>A (NIPBL)	XP_016864818.1:n.*191T>A
XM_017009330.2:c.6630T>A (NIPBL)	XP_016864819.1:p.Thr2210=
XM_017009331.1:c.6621T>A (NIPBL)	XP_016864820.1:p.Thr2207=
XR_925644.2:n.11958A>T (CPLANE1)
NM_133433.4:c.8247T>A (NIPBL) MANE Select	NP_597677.2:p.Thr2749=
NM_015384.5:c.*701T>A (NIPBL)	NP_056199.2:n.*701T>A