Canonical Allele Identifier: CA2685657746
Gene: ASB10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187300_151187301del , CM000669.2:g.151187300_151187301del GRCh38
NC_000007.13:g.150884387_150884388del , CM000669.1:g.150884387_150884388del GRCh37
NC_000007.12:g.150515320_150515321del NCBI36
NG_017016.1:g.5535_5536del

Transcript Alleles

HGVS Amino-acid Change
ENST00000275838.5:c.-168_-167del ENSP00000275838.1:n.-168_-167del
ENST00000377867.7:c.271+154_271+155del ENSP00000367098.3:n.271+154_271+155del
ENST00000415615.1:c.*77_*78del ENSP00000410871.1:n.*77_*78del
NM_001142459.1:c.-168_-167del NP_001135931.2:n.-168_-167del
NM_001142460.1:c.-168_-167del NP_001135932.2:n.-168_-167del
NM_080871.3:c.271+154_271+155del NP_543147.2:n.271+154_271+155del
NM_080871.4:c.271+154_271+155del NP_543147.2:n.271+154_271+155del