Canonical Allele Identifier: CA1752546332
Gene: ASB10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187278A= , CM000669.2:g.151187278A= GRCh38
NC_000007.13:g.150884365A= , CM000669.1:g.150884365A= GRCh37
NC_000007.12:g.150515298A= NCBI36
NG_017016.1:g.5555T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000275838.5:c.-148T= ENSP00000275838.1:n.-148T=
ENST00000377867.7:c.271+174T= ENSP00000367098.3:n.271+174T=
ENST00000415615.1:c.*97T= ENSP00000410871.1:n.*97T=
NM_001142459.1:c.-148T= NP_001135931.2:n.-148T=
NM_001142460.1:c.-148T= NP_001135932.2:n.-148T=
NM_080871.3:c.271+174T= NP_543147.2:n.271+174T=
NM_080871.4:c.271+174T= NP_543147.2:n.271+174T=
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