Canonical Allele Identifier: CA2685657627
Gene: ASB10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151186919del , CM000669.2:g.151186919del GRCh38
NC_000007.13:g.150884006del , CM000669.1:g.150884006del GRCh37
NC_000007.12:g.150514939del NCBI36
NG_017016.1:g.5916del

Transcript Alleles

HGVS Amino-acid change
ENST00000420175.3:c.214del MANE Select ENSP00000391137.2:p.Arg72AlafsTer?
ENST00000275838.5:c.214del ENSP00000275838.1:p.Arg72AlafsTer?
ENST00000377867.7:c.272-258del ENSP00000367098.3:n.272-258del
ENST00000415615.1:c.*258del ENSP00000410871.1:n.*258del
ENST00000420175.2:c.214del ENSP00000391137.2:p.Arg72AlafsTer?
NM_001142459.1:c.214del NP_001135931.2:p.Arg72AlafsTer?
NM_001142460.1:c.214del NP_001135932.2:p.Arg72AlafsTer?
NM_080871.3:c.272-258del NP_543147.2:n.272-258del
XM_005249949.3:c.349del XP_005250006.1:p.Arg117AlafsTer?
NM_001142459.2:c.214del MANE Select NP_001135931.2:p.Arg72AlafsTer?
NM_080871.4:c.272-258del NP_543147.2:n.272-258del