Canonical Allele Identifier: CA2838511000

Gene: NOL6

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.33466042G>T , CM000671.2:g.33466042G>T	GRCh38
NC_000009.11:g.33466040G>T , CM000671.1:g.33466040G>T	GRCh37
NC_000009.10:g.33456040G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297990.9:c.2364+29C>A MANE Select	ENSP00000297990.4:n.2364+29C>A
ENST00000297990.8:c.2364+29C>A	ENSP00000297990.4:n.2364+29C>A
ENST00000353159.6:c.1950+870C>A	ENSP00000313978.4:n.1950+870C>A
ENST00000379471.3:c.2364+29C>A	ENSP00000368784.3:n.2364+29C>A
ENST00000464829.5:n.1680+2738C>A
NM_022917.4:c.2364+29C>A	NP_075068.2:n.2364+29C>A
NM_139235.3:c.1950+870C>A	NP_631981.2:n.1950+870C>A
XM_017015044.2:c.543+29C>A	XP_016870533.1:n.543+29C>A
NM_022917.5:c.2364+29C>A MANE Select	NP_075068.2:n.2364+29C>A
NM_139235.4:c.1950+870C>A	NP_631981.2:n.1950+870C>A