Canonical Allele Identifier: CA2605604353
Gene: ASB10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187335T>C , CM000669.2:g.151187335T>C GRCh38
NC_000007.13:g.150884422T>C , CM000669.1:g.150884422T>C GRCh37
NC_000007.12:g.150515355T>C NCBI36
NG_017016.1:g.5498A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000275838.5:c.-205A>G ENSP00000275838.1:n.-205A>G
ENST00000377867.7:c.271+117A>G ENSP00000367098.3:n.271+117A>G
ENST00000415615.1:c.*40A>G ENSP00000410871.1:n.*40A>G
NM_001142459.1:c.-205A>G NP_001135931.2:n.-205A>G
NM_001142460.1:c.-205A>G NP_001135932.2:n.-205A>G
NM_080871.3:c.271+117A>G NP_543147.2:n.271+117A>G
NM_080871.4:c.271+117A>G NP_543147.2:n.271+117A>G