Canonical Allele Identifier: CA2685657625
Gene: ASB10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151186819_151186820del , CM000669.2:g.151186819_151186820del GRCh38
NC_000007.13:g.150883906_150883907del , CM000669.1:g.150883906_150883907del GRCh37
NC_000007.12:g.150514839_150514840del NCBI36
NG_017016.1:g.6015_6016del

Transcript Alleles

HGVS Amino-acid change
ENST00000420175.3:c.313_314del MANE Select ENSP00000391137.2:p.Leu105GlufsTer?
ENST00000275838.5:c.313_314del ENSP00000275838.1:p.Leu105GlufsTer?
ENST00000377867.7:c.272-159_272-158del ENSP00000367098.3:n.272-159_272-158del
ENST00000415615.1:c.*357_*358del ENSP00000410871.1:n.*357_*358del
ENST00000420175.2:c.313_314del ENSP00000391137.2:p.Leu105GlufsTer?
NM_001142459.1:c.313_314del NP_001135931.2:p.Leu105GlufsTer?
NM_001142460.1:c.313_314del NP_001135932.2:p.Leu105GlufsTer?
NM_080871.3:c.272-159_272-158del NP_543147.2:n.272-159_272-158del
XM_005249949.3:c.448_449del XP_005250006.1:p.Leu150GlufsTer?
NM_001142459.2:c.313_314del MANE Select NP_001135931.2:p.Leu105GlufsTer?
NM_080871.4:c.272-159_272-158del NP_543147.2:n.272-159_272-158del