Canonical Allele Identifier: CA1752546302
Gene: ASB10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187270C= , CM000669.2:g.151187270C= GRCh38
NC_000007.13:g.150884357C= , CM000669.1:g.150884357C= GRCh37
NC_000007.12:g.150515290C= NCBI36
NG_017016.1:g.5563G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000275838.5:c.-140G= ENSP00000275838.1:n.-140G=
ENST00000377867.7:c.271+182G= ENSP00000367098.3:n.271+182G=
ENST00000415615.1:c.*105G= ENSP00000410871.1:n.*105G=
NM_001142459.1:c.-140G= NP_001135931.2:n.-140G=
NM_001142460.1:c.-140G= NP_001135932.2:n.-140G=
NM_080871.3:c.271+182G= NP_543147.2:n.271+182G=
NM_080871.4:c.271+182G= NP_543147.2:n.271+182G=
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