Canonical Allele Identifier: CA2685657515
Gene: ASB10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151186427del , CM000669.2:g.151186427del GRCh38
NC_000007.13:g.150883514del , CM000669.1:g.150883514del GRCh37
NC_000007.12:g.150514447del NCBI36
NG_017016.1:g.6410del

Transcript Alleles

HGVS Amino-acid Change
ENST00000420175.3:c.553del MANE Select ENSP00000391137.2:p.Leu185CysfsTer?
ENST00000275838.5:c.553del ENSP00000275838.1:p.Leu185CysfsTer?
ENST00000377867.7:c.508del ENSP00000367098.3:p.Leu170CysfsTer?
ENST00000420175.2:c.553del ENSP00000391137.2:p.Leu185CysfsTer?
NM_001142459.1:c.553del NP_001135931.2:p.Leu185CysfsTer?
NM_001142460.1:c.553del NP_001135932.2:p.Leu185CysfsTer?
NM_080871.3:c.508del NP_543147.2:p.Leu170CysfsTer?
XM_005249949.3:c.688del XP_005250006.1:p.Leu230CysfsTer?
NM_001142459.2:c.553del MANE Select NP_001135931.2:p.Leu185CysfsTer?
NM_080871.4:c.508del NP_543147.2:p.Leu170CysfsTer?