Canonical Allele Identifier: CA370037967
Gene: ASB10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187058C>T , CM000669.2:g.151187058C>T GRCh38
NC_000007.13:g.150884145C>T , CM000669.1:g.150884145C>T GRCh37
NC_000007.12:g.150515078C>T NCBI36
NG_017016.1:g.5775G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000420175.3:c.73G>A MANE Select ENSP00000391137.2:p.Ala25Thr
ENST00000275838.5:c.73G>A ENSP00000275838.1:p.Ala25Thr
ENST00000377867.7:c.271+394G>A ENSP00000367098.3:n.271+394G>A
ENST00000415615.1:c.*122-5G>A ENSP00000410871.1:n.*122-5G>A
ENST00000420175.2:c.73G>A ENSP00000391137.2:p.Ala25Thr
NM_001142459.1:c.73G>A NP_001135931.2:p.Ala25Thr
NM_001142460.1:c.73G>A NP_001135932.2:p.Ala25Thr
NM_080871.3:c.271+394G>A NP_543147.2:n.271+394G>A
XM_005249949.3:c.208G>A XP_005250006.1:p.Ala70Thr
NM_001142459.2:c.73G>A MANE Select NP_001135931.2:p.Ala25Thr
NM_080871.4:c.271+394G>A NP_543147.2:n.271+394G>A