Canonical Allele Identifier: CA1752545636
Gene: ASB10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151186926A= , CM000669.2:g.151186926A= GRCh38
NC_000007.13:g.150884013A= , CM000669.1:g.150884013A= GRCh37
NC_000007.12:g.150514946A= NCBI36
NG_017016.1:g.5907T=

Transcript Alleles

HGVS Amino-acid change
ENST00000420175.3:c.205T= MANE Select ENSP00000391137.2:p.Cys69=
ENST00000275838.5:c.205T= ENSP00000275838.1:p.Cys69=
ENST00000377867.7:c.272-267T= ENSP00000367098.3:n.272-267T=
ENST00000415615.1:c.*249T= ENSP00000410871.1:n.*249T=
ENST00000420175.2:c.205T= ENSP00000391137.2:p.Cys69=
NM_001142459.1:c.205T= NP_001135931.2:p.Cys69=
NM_001142460.1:c.205T= NP_001135932.2:p.Cys69=
NM_080871.3:c.272-267T= NP_543147.2:n.272-267T=
XM_005249949.3:c.340T= XP_005250006.1:p.Cys114=
NM_001142459.2:c.205T= MANE Select NP_001135931.2:p.Cys69=
NM_080871.4:c.272-267T= NP_543147.2:n.272-267T=