Canonical Allele Identifier: CA2685657516
Gene: ASB10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151186432del , CM000669.2:g.151186432del GRCh38
NC_000007.13:g.150883519del , CM000669.1:g.150883519del GRCh37
NC_000007.12:g.150514452del NCBI36
NG_017016.1:g.6403del

Transcript Alleles

HGVS Amino-acid Change
ENST00000420175.3:c.546del MANE Select ENSP00000391137.2:p.Lys182AsnfsTer?
ENST00000275838.5:c.546del ENSP00000275838.1:p.Lys182AsnfsTer?
ENST00000377867.7:c.501del ENSP00000367098.3:p.Lys167AsnfsTer?
ENST00000420175.2:c.546del ENSP00000391137.2:p.Lys182AsnfsTer?
NM_001142459.1:c.546del NP_001135931.2:p.Lys182AsnfsTer?
NM_001142460.1:c.546del NP_001135932.2:p.Lys182AsnfsTer?
NM_080871.3:c.501del NP_543147.2:p.Lys167AsnfsTer?
XM_005249949.3:c.681del XP_005250006.1:p.Lys227AsnfsTer?
NM_001142459.2:c.546del MANE Select NP_001135931.2:p.Lys182AsnfsTer?
NM_080871.4:c.501del NP_543147.2:p.Lys167AsnfsTer?