Canonical Allele Identifier: CA2685657668

Gene: ASB10

Linked Data

• gnomAD v4: 7-151187179-C-CAT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187180_151187181insTA , CM000669.2:g.151187180_151187181insTA	GRCh38
NC_000007.13:g.150884267_150884268insTA , CM000669.1:g.150884267_150884268insTA	GRCh37
NC_000007.12:g.150515200_150515201insTA	NCBI36
NG_017016.1:g.5653_5654insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.-50_-49insAT MANE Select	ENSP00000391137.2:n.-50_-49insAT
ENST00000275838.5:c.-50_-49insAT	ENSP00000275838.1:n.-50_-49insAT
ENST00000377867.7:c.271+272_271+273insAT	ENSP00000367098.3:n.271+272_271+273insAT
ENST00000415615.1:c.*121+74_*121+75insAT	ENSP00000410871.1:n.*121+74_*121+75insAT
NM_001142459.1:c.-50_-49insAT	NP_001135931.2:n.-50_-49insAT
NM_001142460.1:c.-50_-49insAT	NP_001135932.2:n.-50_-49insAT
NM_080871.3:c.271+272_271+273insAT	NP_543147.2:n.271+272_271+273insAT
XM_005249949.3:c.86_87insAT	XP_005250006.1:p.Pro30CysfsTer20
NM_001142459.2:c.-50_-49insAT MANE Select	NP_001135931.2:n.-50_-49insAT
NM_080871.4:c.271+272_271+273insAT	NP_543147.2:n.271+272_271+273insAT