Canonical Allele Identifier: CA2739944788
Gene: ASB10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187256G>T , CM000669.2:g.151187256G>T GRCh38
NC_000007.13:g.150884343G>T , CM000669.1:g.150884343G>T GRCh37
NC_000007.12:g.150515276G>T NCBI36
NG_017016.1:g.5577C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000275838.5:c.-126C>A ENSP00000275838.1:n.-126C>A
ENST00000377867.7:c.271+196C>A ENSP00000367098.3:n.271+196C>A
ENST00000415615.1:c.*119C>A ENSP00000410871.1:n.*119C>A
NM_001142459.1:c.-126C>A NP_001135931.2:n.-126C>A
NM_001142460.1:c.-126C>A NP_001135932.2:n.-126C>A
NM_080871.3:c.271+196C>A NP_543147.2:n.271+196C>A
XM_005249949.3:c.10C>A XP_005250006.1:p.Gln4Lys
NM_080871.4:c.271+196C>A NP_543147.2:n.271+196C>A