Canonical Allele Identifier: CA413550729

Gene: NONO

Linked Data

• ClinVar Variation Id: 1804718
• ClinVar RCV Id: RCV002470015
• MyVariant Identifiers: chrX:g.70519918C>T (hg19) ; chrX:g.71300068C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300068C>T , CM000685.2:g.71300068C>T	GRCh38
NC_000023.10:g.70519918C>T , CM000685.1:g.70519918C>T	GRCh37
NC_000023.9:g.70436643C>T	NCBI36
NG_046742.1:g.21877C>T
NG_054891.1:g.3794C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1408C>T MANE Select	ENSP00000276079.8:p.Arg470Ter
ENST00000373856.8:c.1506C>T	ENSP00000362963.4:p.Ala502=
ENST00000420903.6:c.1408C>T	ENSP00000410299.2:p.Arg470Ter
ENST00000450092.6:c.1408C>T	ENSP00000415777.2:p.Arg470Ter
ENST00000454976.2:c.1408C>T	ENSP00000406673.2:p.Arg470Ter
ENST00000473525.2:n.2116C>T
ENST00000676495.1:n.2819C>T
ENST00000676499.1:n.2364C>T
ENST00000676797.1:c.1141C>T	ENSP00000503920.1:p.Arg381Ter
ENST00000677014.1:c.*1235C>T	ENSP00000503813.1:n.*1235C>T
ENST00000677218.1:n.2579C>T
ENST00000677245.1:c.*1617C>T	ENSP00000503929.1:n.*1617C>T
ENST00000677274.1:c.1408C>T	ENSP00000504314.1:p.Arg470Ter
ENST00000677446.1:c.1408C>T	ENSP00000503031.1:p.Arg470Ter
ENST00000677612.1:c.1408C>T	ENSP00000504351.1:p.Arg470Ter
ENST00000677766.1:n.3813C>T
ENST00000677826.1:n.2150C>T
ENST00000677879.1:c.1228C>T	ENSP00000504090.1:p.Arg410Ter
ENST00000677977.1:n.3240C>T
ENST00000678231.1:c.1408C>T	ENSP00000503233.1:p.Arg470Ter
ENST00000678323.1:n.2506C>T
ENST00000678335.1:c.*321C>T	ENSP00000503769.1:n.*321C>T
ENST00000678437.1:c.1399C>T	ENSP00000504007.1:p.Arg467Ter
ENST00000678660.1:c.1423C>T	ENSP00000504665.1:p.Arg475Ter
ENST00000678830.1:c.1498C>T	ENSP00000504263.1:p.Arg500Ter
ENST00000679029.1:c.*222C>T	ENSP00000504193.1:n.*222C>T
ENST00000679267.1:n.3615C>T
ENST00000276079.12:c.1408C>T	ENSP00000276079.8:p.Arg470Ter
ENST00000373841.5:c.1408C>T	ENSP00000362947.1:p.Arg470Ter
ENST00000373856.7:c.1408C>T	ENSP00000362963.3:p.Arg470Ter
ENST00000472185.1:n.61-451C>T
ENST00000473525.1:n.1182C>T
ENST00000474431.5:n.443C>T
ENST00000490044.5:n.2115C>T
ENST00000535149.5:c.1141C>T	ENSP00000441364.1:p.Arg381Ter
NM_001145408.1:c.1408C>T	NP_001138880.1:p.Arg470Ter
NM_001145409.1:c.1408C>T	NP_001138881.1:p.Arg470Ter
NM_001145410.1:c.1141C>T	NP_001138882.1:p.Arg381Ter
NM_007363.4:c.1408C>T	NP_031389.3:p.Arg470Ter
NM_007363.5:c.1408C>T MANE Select	NP_031389.3:p.Arg470Ter
NM_001145408.2:c.1408C>T	NP_001138880.1:p.Arg470Ter
NM_001145409.2:c.1408C>T	NP_001138881.1:p.Arg470Ter
NM_001145410.2:c.1141C>T	NP_001138882.1:p.Arg381Ter