Canonical Allele Identifier: CA1752545608
Gene: ASB10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151186909G= , CM000669.2:g.151186909G= GRCh38
NC_000007.13:g.150883996G= , CM000669.1:g.150883996G= GRCh37
NC_000007.12:g.150514929G= NCBI36
NG_017016.1:g.5924C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000420175.3:c.222C= MANE Select ENSP00000391137.2:p.Leu74=
ENST00000275838.5:c.222C= ENSP00000275838.1:p.Leu74=
ENST00000377867.7:c.272-250C= ENSP00000367098.3:n.272-250C=
ENST00000415615.1:c.*266C= ENSP00000410871.1:n.*266C=
ENST00000420175.2:c.222C= ENSP00000391137.2:p.Leu74=
NM_001142459.1:c.222C= NP_001135931.2:p.Leu74=
NM_001142460.1:c.222C= NP_001135932.2:p.Leu74=
NM_080871.3:c.272-250C= NP_543147.2:n.272-250C=
XM_005249949.3:c.357C= XP_005250006.1:p.Leu119=
NM_001142459.2:c.222C= MANE Select NP_001135931.2:p.Leu74=
NM_080871.4:c.272-250C= NP_543147.2:n.272-250C=