Canonical Allele Identifier: CA1752544786
Gene: ASB10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151186409C= , CM000669.2:g.151186409C= GRCh38
NC_000007.13:g.150883496C= , CM000669.1:g.150883496C= GRCh37
NC_000007.12:g.150514429C= NCBI36
NG_017016.1:g.6424G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000420175.3:c.567G= MANE Select ENSP00000391137.2:p.Arg189=
ENST00000275838.5:c.567G= ENSP00000275838.1:p.Arg189=
ENST00000377867.7:c.522G= ENSP00000367098.3:p.Arg174=
ENST00000420175.2:c.567G= ENSP00000391137.2:p.Arg189=
NM_001142459.1:c.567G= NP_001135931.2:p.Arg189=
NM_001142460.1:c.567G= NP_001135932.2:p.Arg189=
NM_080871.3:c.522G= NP_543147.2:p.Arg174=
XM_005249949.3:c.702G= XP_005250006.1:p.Arg234=
NM_001142459.2:c.567G= MANE Select NP_001135931.2:p.Arg189=
NM_080871.4:c.522G= NP_543147.2:p.Arg174=