Canonical Allele Identifier: CA1752546429
Gene: ASB10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187326G= , CM000669.2:g.151187326G= GRCh38
NC_000007.13:g.150884413G= , CM000669.1:g.150884413G= GRCh37
NC_000007.12:g.150515346G= NCBI36
NG_017016.1:g.5507C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000275838.5:c.-196C= ENSP00000275838.1:n.-196C=
ENST00000377867.7:c.271+126C= ENSP00000367098.3:n.271+126C=
ENST00000415615.1:c.*49C= ENSP00000410871.1:n.*49C=
NM_001142459.1:c.-196C= NP_001135931.2:n.-196C=
NM_001142460.1:c.-196C= NP_001135932.2:n.-196C=
NM_080871.3:c.271+126C= NP_543147.2:n.271+126C=
NM_080871.4:c.271+126C= NP_543147.2:n.271+126C=
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