Canonical Allele Identifier: CA2579066576
Gene: ASB10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187311A>G , CM000669.2:g.151187311A>G GRCh38
NC_000007.13:g.150884398A>G , CM000669.1:g.150884398A>G GRCh37
NC_000007.12:g.150515331A>G NCBI36
NG_017016.1:g.5522T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000275838.5:c.-181T>C ENSP00000275838.1:n.-181T>C
ENST00000377867.7:c.271+141T>C ENSP00000367098.3:n.271+141T>C
ENST00000415615.1:c.*64T>C ENSP00000410871.1:n.*64T>C
NM_001142459.1:c.-181T>C NP_001135931.2:n.-181T>C
NM_001142460.1:c.-181T>C NP_001135932.2:n.-181T>C
NM_080871.3:c.271+141T>C NP_543147.2:n.271+141T>C
NM_080871.4:c.271+141T>C NP_543147.2:n.271+141T>C