Canonical Allele Identifier: CA10446222

Gene: NONO

Linked Data

• dbSNP Id: rs780470033
• ExAC: X:70519954 CCCTTAAAAGAAGGACCCTTTTTG / C
• gnomAD v2: X-70519954-CCCTTAAAAGAAGGACCCTTTTTG-C
• gnomAD v4: X-71300104-CCCTTAAAAGAAGGACCCTTTTTG-C
• MyVariant Identifiers: chrX:g.70519955_70519977del (hg19) ; chrX:g.71300105_71300127del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71300105_71300127del , CM000685.2:g.71300105_71300127del	GRCh38
NC_000023.10:g.70519955_70519977del , CM000685.1:g.70519955_70519977del	GRCh37
NC_000023.9:g.70436680_70436702del	NCBI36
NG_046742.1:g.21914_21936del
NG_054891.1:g.3831_3853del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.*29_*51del MANE Select	ENSP00000276079.8:n.*29_*51del
ENST00000420903.6:c.*29_*51del	ENSP00000410299.2:n.*29_*51del
ENST00000473525.2:n.2153_2175del
ENST00000676495.1:n.2856_2878del
ENST00000676499.1:n.2401_2423del
ENST00000676797.1:c.*29_*51del	ENSP00000503920.1:n.*29_*51del
ENST00000677014.1:c.*1272_*1294del	ENSP00000503813.1:n.*1272_*1294del
ENST00000677218.1:n.2616_2638del
ENST00000677245.1:c.*1654_*1676del	ENSP00000503929.1:n.*1654_*1676del
ENST00000677274.1:c.*29_*51del	ENSP00000504314.1:n.*29_*51del
ENST00000677446.1:c.*29_*51del	ENSP00000503031.1:n.*29_*51del
ENST00000677612.1:c.*29_*51del	ENSP00000504351.1:n.*29_*51del
ENST00000677766.1:n.3850_3872del
ENST00000677826.1:n.2187_2209del
ENST00000677879.1:c.*29_*51del	ENSP00000504090.1:n.*29_*51del
ENST00000677977.1:n.3277_3299del
ENST00000678231.1:c.*29_*51del	ENSP00000503233.1:n.*29_*51del
ENST00000678323.1:n.2543_2565del
ENST00000678335.1:c.*358_*380del	ENSP00000503769.1:n.*358_*380del
ENST00000678437.1:c.*29_*51del	ENSP00000504007.1:n.*29_*51del
ENST00000678660.1:c.*29_*51del	ENSP00000504665.1:n.*29_*51del
ENST00000678830.1:c.*29_*51del	ENSP00000504263.1:n.*29_*51del
ENST00000679029.1:c.*259_*281del	ENSP00000504193.1:n.*259_*281del
ENST00000679267.1:n.3652_3674del
ENST00000276079.12:c.*29_*51del	ENSP00000276079.8:n.*29_*51del
ENST00000373841.5:c.*29_*51del	ENSP00000362947.1:n.*29_*51del
ENST00000373856.7:c.*29_*51del	ENSP00000362963.3:n.*29_*51del
ENST00000472185.1:n.61-414_61-392del
ENST00000473525.1:n.1219_1241del
ENST00000474431.5:n.480_502del
ENST00000490044.5:n.2152_2174del
ENST00000535149.5:c.*29_*51del	ENSP00000441364.1:n.*29_*51del
NM_001145408.1:c.*29_*51del	NP_001138880.1:n.*29_*51del
NM_001145409.1:c.*29_*51del	NP_001138881.1:n.*29_*51del
NM_001145410.1:c.*29_*51del	NP_001138882.1:n.*29_*51del
NM_007363.4:c.*29_*51del	NP_031389.3:n.*29_*51del
NM_007363.5:c.*29_*51del MANE Select	NP_031389.3:n.*29_*51del
NM_001145408.2:c.*29_*51del	NP_001138880.1:n.*29_*51del
NM_001145409.2:c.*29_*51del	NP_001138881.1:n.*29_*51del
NM_001145410.2:c.*29_*51del	NP_001138882.1:n.*29_*51del