Canonical Allele Identifier: CA1752546466
Gene: ASB10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187352C= , CM000669.2:g.151187352C= GRCh38
NC_000007.13:g.150884439C= , CM000669.1:g.150884439C= GRCh37
NC_000007.12:g.150515372C= NCBI36
NG_017016.1:g.5481G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000275838.5:c.-222G= ENSP00000275838.1:n.-222G=
ENST00000377867.7:c.271+100G= ENSP00000367098.3:n.271+100G=
ENST00000415615.1:c.*23G= ENSP00000410871.1:n.*23G=
NM_001142459.1:c.-222G= NP_001135931.2:n.-222G=
NM_001142460.1:c.-222G= NP_001135932.2:n.-222G=
NM_080871.3:c.271+100G= NP_543147.2:n.271+100G=
NM_080871.4:c.271+100G= NP_543147.2:n.271+100G=
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