Canonical Allele Identifier: CA1752545631
Gene: ASB10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151186924A= , CM000669.2:g.151186924A= GRCh38
NC_000007.13:g.150884011A= , CM000669.1:g.150884011A= GRCh37
NC_000007.12:g.150514944A= NCBI36
NG_017016.1:g.5909T=

Transcript Alleles

HGVS Amino-acid change
ENST00000420175.3:c.207T= MANE Select ENSP00000391137.2:p.Cys69=
ENST00000275838.5:c.207T= ENSP00000275838.1:p.Cys69=
ENST00000377867.7:c.272-265T= ENSP00000367098.3:n.272-265T=
ENST00000415615.1:c.*251T= ENSP00000410871.1:n.*251T=
ENST00000420175.2:c.207T= ENSP00000391137.2:p.Cys69=
NM_001142459.1:c.207T= NP_001135931.2:p.Cys69=
NM_001142460.1:c.207T= NP_001135932.2:p.Cys69=
NM_080871.3:c.272-265T= NP_543147.2:n.272-265T=
XM_005249949.3:c.342T= XP_005250006.1:p.Cys114=
NM_001142459.2:c.207T= MANE Select NP_001135931.2:p.Cys69=
NM_080871.4:c.272-265T= NP_543147.2:n.272-265T=