Canonical Allele Identifier: CA4574028
Gene: ASB10 HGNC NCBI

Linked Data

dbSNP Id: rs34383739

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187192_151187197del , CM000669.2:g.151187192_151187197del GRCh38
NC_000007.13:g.150884279_150884284del , CM000669.1:g.150884279_150884284del GRCh37
NC_000007.12:g.150515212_150515217del NCBI36
NG_017016.1:g.5648_5653del

Transcript Alleles

HGVS Amino-acid Change
ENST00000420175.3:c.-55_-50del MANE Select ENSP00000391137.2:n.-55_-50del
ENST00000275838.5:c.-55_-50del ENSP00000275838.1:n.-55_-50del
ENST00000377867.7:c.271+267_271+272del ENSP00000367098.3:n.271+267_271+272del
ENST00000415615.1:c.*121+69_*121+74del ENSP00000410871.1:n.*121+69_*121+74del
NM_001142459.1:c.-55_-50del NP_001135931.2:n.-55_-50del
NM_001142460.1:c.-55_-50del NP_001135932.2:n.-55_-50del
NM_080871.3:c.271+267_271+272del NP_543147.2:n.271+267_271+272del
XM_005249949.3:c.81_86del XP_005250006.1:p.Ser28_Leu29del
NM_001142459.2:c.-55_-50del MANE Select NP_001135931.2:n.-55_-50del
NM_080871.4:c.271+267_271+272del NP_543147.2:n.271+267_271+272del