Canonical Allele Identifier: CA370035622
Gene: ASB10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151186392T>A , CM000669.2:g.151186392T>A GRCh38
NC_000007.13:g.150883479T>A , CM000669.1:g.150883479T>A GRCh37
NC_000007.12:g.150514412T>A NCBI36
NG_017016.1:g.6441A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000420175.3:c.584A>T MANE Select ENSP00000391137.2:p.Glu195Val
ENST00000275838.5:c.584A>T ENSP00000275838.1:p.Glu195Val
ENST00000377867.7:c.539A>T ENSP00000367098.3:p.Glu180Val
ENST00000420175.2:c.584A>T ENSP00000391137.2:p.Glu195Val
NM_001142459.1:c.584A>T NP_001135931.2:p.Glu195Val
NM_001142460.1:c.584A>T NP_001135932.2:p.Glu195Val
NM_080871.3:c.539A>T NP_543147.2:p.Glu180Val
XM_005249949.3:c.719A>T XP_005250006.1:p.Glu240Val
NM_001142459.2:c.584A>T MANE Select NP_001135931.2:p.Glu195Val
NM_080871.4:c.539A>T NP_543147.2:p.Glu180Val