Canonical Allele Identifier: CA2694039277

Gene: NONO

Linked Data

• gnomAD v4: X-71300265-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300265T>C , CM000685.2:g.71300265T>C	GRCh38
NC_000023.10:g.70520115T>C , CM000685.1:g.70520115T>C	GRCh37
NC_000023.9:g.70436840T>C	NCBI36
NG_046742.1:g.22074T>C
NG_054891.1:g.3991T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.*189T>C MANE Select	ENSP00000276079.8:n.*189T>C
ENST00000420903.6:c.*189T>C	ENSP00000410299.2:n.*189T>C
ENST00000473525.2:n.2313T>C
ENST00000676495.1:n.3016T>C
ENST00000676499.1:n.2561T>C
ENST00000676797.1:c.*189T>C	ENSP00000503920.1:n.*189T>C
ENST00000677014.1:c.*1432T>C	ENSP00000503813.1:n.*1432T>C
ENST00000677218.1:n.2776T>C
ENST00000677245.1:c.*1814T>C	ENSP00000503929.1:n.*1814T>C
ENST00000677274.1:c.*189T>C	ENSP00000504314.1:n.*189T>C
ENST00000677446.1:c.*189T>C	ENSP00000503031.1:n.*189T>C
ENST00000677612.1:c.*189T>C	ENSP00000504351.1:n.*189T>C
ENST00000677766.1:n.4010T>C
ENST00000677826.1:n.2347T>C
ENST00000677879.1:c.*189T>C	ENSP00000504090.1:n.*189T>C
ENST00000677977.1:n.3437T>C
ENST00000678231.1:c.*189T>C	ENSP00000503233.1:n.*189T>C
ENST00000678323.1:n.2703T>C
ENST00000678335.1:c.*518T>C	ENSP00000503769.1:n.*518T>C
ENST00000678437.1:c.*189T>C	ENSP00000504007.1:n.*189T>C
ENST00000678660.1:c.*189T>C	ENSP00000504665.1:n.*189T>C
ENST00000678830.1:c.*189T>C	ENSP00000504263.1:n.*189T>C
ENST00000679029.1:c.*419T>C	ENSP00000504193.1:n.*419T>C
ENST00000679267.1:n.3812T>C
ENST00000276079.12:c.*189T>C	ENSP00000276079.8:n.*189T>C
ENST00000373841.5:c.*189T>C	ENSP00000362947.1:n.*189T>C
ENST00000373856.7:c.*189T>C	ENSP00000362963.3:n.*189T>C
ENST00000472185.1:n.61-254T>C
ENST00000473525.1:n.1379T>C
ENST00000474431.5:n.640T>C
ENST00000490044.5:n.2312T>C
ENST00000535149.5:c.*189T>C	ENSP00000441364.1:n.*189T>C
NM_001145408.1:c.*189T>C	NP_001138880.1:n.*189T>C
NM_001145409.1:c.*189T>C	NP_001138881.1:n.*189T>C
NM_001145410.1:c.*189T>C	NP_001138882.1:n.*189T>C
NM_007363.4:c.*189T>C	NP_031389.3:n.*189T>C
NM_007363.5:c.*189T>C MANE Select	NP_031389.3:n.*189T>C
NM_001145408.2:c.*189T>C	NP_001138880.1:n.*189T>C
NM_001145409.2:c.*189T>C	NP_001138881.1:n.*189T>C
NM_001145410.2:c.*189T>C	NP_001138882.1:n.*189T>C