Canonical Allele Identifier: CA2685657670

Gene: ASB10

Linked Data

• gnomAD v4: 7-151187179-C-CGG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187179_151187180insGG , CM000669.2:g.151187179_151187180insGG	GRCh38
NC_000007.13:g.150884266_150884267insGG , CM000669.1:g.150884266_150884267insGG	GRCh37
NC_000007.12:g.150515199_150515200insGG	NCBI36
NG_017016.1:g.5653_5654insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.-50_-49insCC MANE Select	ENSP00000391137.2:n.-50_-49insCC
ENST00000275838.5:c.-50_-49insCC	ENSP00000275838.1:n.-50_-49insCC
ENST00000377867.7:c.271+272_271+273insCC	ENSP00000367098.3:n.271+272_271+273insCC
ENST00000415615.1:c.*121+74_*121+75insCC	ENSP00000410871.1:n.*121+74_*121+75insCC
NM_001142459.1:c.-50_-49insCC	NP_001135931.2:n.-50_-49insCC
NM_001142460.1:c.-50_-49insCC	NP_001135932.2:n.-50_-49insCC
NM_080871.3:c.271+272_271+273insCC	NP_543147.2:n.271+272_271+273insCC
XM_005249949.3:c.86_87insCC	XP_005250006.1:p.Pro30ArgfsTer20
NM_001142459.2:c.-50_-49insCC MANE Select	NP_001135931.2:n.-50_-49insCC
NM_080871.4:c.271+272_271+273insCC	NP_543147.2:n.271+272_271+273insCC