Canonical Allele Identifier: CA2839546399

Gene: NUBPL

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.31624326T>G , CM000676.2:g.31624326T>G	GRCh38
NC_000014.8:g.32093532T>G , CM000676.1:g.32093532T>G	GRCh37
NC_000014.7:g.31163283T>G	NCBI36
NG_028349.1:g.67942T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281081.12:c.382+24947T>G MANE Select	ENSP00000281081.7:n.382+24947T>G
ENST00000281081.11:c.382+24947T>G	ENSP00000281081.7:n.382+24947T>G
ENST00000547839.5:c.382+24947T>G	ENSP00000449918.1:n.382+24947T>G
ENST00000548937.5:n.386+24947T>G
ENST00000549838.5:c.346+24947T>G	ENSP00000447658.1:n.346+24947T>G
ENST00000550355.1:n.331+24947T>G
ENST00000550649.5:c.291+59278T>G	ENSP00000447618.1:n.291+59278T>G
ENST00000551314.1:c.226+24947T>G	ENSP00000447234.1:n.226+24947T>G
ENST00000552489.5:c.476+24947T>G	ENSP00000447316.1:n.476+24947T>G
NM_001201573.1:c.94+24947T>G	NP_001188502.1:n.94+24947T>G
NM_025152.2:c.382+24947T>G	NP_079428.2:n.382+24947T>G
NR_120408.1:n.437+24947T>G
XM_005268099.3:c.382+24947T>G	XP_005268156.1:n.382+24947T>G
XM_011537181.1:c.107+24947T>G	XP_011535483.1:n.107+24947T>G
XM_011537182.1:c.-74+24947T>G	XP_011535484.1:n.-74+24947T>G
XM_011537183.1:c.382+24947T>G	XP_011535485.1:n.382+24947T>G
XM_011537181.2:c.107+24947T>G	XP_011535483.1:n.107+24947T>G
XM_011537182.2:c.-74+24947T>G	XP_011535484.1:n.-74+24947T>G
XM_011537183.2:c.382+24947T>G	XP_011535485.1:n.382+24947T>G
XM_017021664.1:c.382+24947T>G	XP_016877153.1:n.382+24947T>G
XM_017021665.2:c.382+24947T>G	XP_016877154.1:n.382+24947T>G
XM_017021666.1:c.382+24947T>G	XP_016877155.1:n.382+24947T>G
XM_017021667.1:c.-2+24947T>G	XP_016877156.1:n.-2+24947T>G
NM_025152.3:c.382+24947T>G MANE Select	NP_079428.2:n.382+24947T>G
NR_120408.2:n.418+24947T>G
NM_001201573.2:c.94+24947T>G	NP_001188502.1:n.94+24947T>G