Canonical Allele Identifier: CA1752546391
Gene: ASB10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187312_151187327delinsAGGTGTAGGCTATTGG , CM000669.2:g.151187312_151187327delinsAGGTGTAGGCTATTGG GRCh38
NC_000007.13:g.150884399_150884414delinsAGGTGTAGGCTATTGG , CM000669.1:g.150884399_150884414delinsAGGTGTAGGCTATTGG GRCh37
NC_000007.12:g.150515332_150515347delinsAGGTGTAGGCTATTGG NCBI36
NG_017016.1:g.5506_5521delinsCCAATAGCCTACACCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000275838.5:c.-197_-182delinsCCAATAGCCTACACCT ENSP00000275838.1:n.-197_-182delinsCCAATAGCCTACACCT
ENST00000377867.7:c.271+125_271+140delinsCCAATAGCCTACACCT ENSP00000367098.3:n.271+125_271+140delinsCCAATAGCCTACACCT
ENST00000415615.1:c.*48_*63delinsCCAATAGCCTACACCT ENSP00000410871.1:n.*48_*63delinsCCAATAGCCTACACCT
NM_001142459.1:c.-197_-182delinsCCAATAGCCTACACCT NP_001135931.2:n.-197_-182delinsCCAATAGCCTACACCT
NM_001142460.1:c.-197_-182delinsCCAATAGCCTACACCT NP_001135932.2:n.-197_-182delinsCCAATAGCCTACACCT
NM_080871.3:c.271+125_271+140delinsCCAATAGCCTACACCT NP_543147.2:n.271+125_271+140delinsCCAATAGCCTACACCT
NM_080871.4:c.271+125_271+140delinsCCAATAGCCTACACCT NP_543147.2:n.271+125_271+140delinsCCAATAGCCTACACCT