Canonical Allele Identifier: CA1752546387
Gene: ASB10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187309_151187311delinsCCA , CM000669.2:g.151187309_151187311delinsCCA GRCh38
NC_000007.13:g.150884396_150884398delinsCCA , CM000669.1:g.150884396_150884398delinsCCA GRCh37
NC_000007.12:g.150515329_150515331delinsCCA NCBI36
NG_017016.1:g.5522_5524delinsTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000275838.5:c.-181_-179delinsTGG ENSP00000275838.1:n.-181_-179delinsTGG
ENST00000377867.7:c.271+141_271+143delinsTGG ENSP00000367098.3:n.271+141_271+143delinsTGG
ENST00000415615.1:c.*64_*66delinsTGG ENSP00000410871.1:n.*64_*66delinsTGG
NM_001142459.1:c.-181_-179delinsTGG NP_001135931.2:n.-181_-179delinsTGG
NM_001142460.1:c.-181_-179delinsTGG NP_001135932.2:n.-181_-179delinsTGG
NM_080871.3:c.271+141_271+143delinsTGG NP_543147.2:n.271+141_271+143delinsTGG
NM_080871.4:c.271+141_271+143delinsTGG NP_543147.2:n.271+141_271+143delinsTGG