Canonical Allele Identifier: CA1752545957
Gene: ASB10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187130_151187131delinsTG , CM000669.2:g.151187130_151187131delinsTG GRCh38
NC_000007.13:g.150884217_150884218delinsTG , CM000669.1:g.150884217_150884218delinsTG GRCh37
NC_000007.12:g.150515150_150515151delinsTG NCBI36
NG_017016.1:g.5702_5703delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000420175.3:c.-1_1delinsCA
ENST00000275838.5:c.-1_1delinsCA
ENST00000377867.7:c.271+321_271+322delinsCA ENSP00000367098.3:n.271+321_271+322delinsCA
ENST00000415615.1:c.*122-78_*122-77delinsCA ENSP00000410871.1:n.*122-78_*122-77delinsCA
ENST00000420175.2:c.-1_1delinsCA
NM_001142459.1:c.-1_1delinsCA
NM_001142460.1:c.-1_1delinsCA
NM_080871.3:c.271+321_271+322delinsCA NP_543147.2:n.271+321_271+322delinsCA
XM_005249949.3:c.135_136delinsCA XP_005250006.1:p.His45=
NM_001142459.2:c.-1_1delinsCA
NM_080871.4:c.271+321_271+322delinsCA NP_543147.2:n.271+321_271+322delinsCA