Canonical Allele Identifier: CA1752544555
Gene: ASB10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151186182G= , CM000669.2:g.151186182G= GRCh38
NC_000007.13:g.150883269G= , CM000669.1:g.150883269G= GRCh37
NC_000007.12:g.150514202G= NCBI36
NG_017016.1:g.6651C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000420175.3:c.584+210C= MANE Select ENSP00000391137.2:n.584+210C=
ENST00000275838.5:c.584+210C= ENSP00000275838.1:n.584+210C=
ENST00000377867.7:c.539+210C= ENSP00000367098.3:n.539+210C=
ENST00000420175.2:c.584+210C= ENSP00000391137.2:n.584+210C=
NM_001142459.1:c.584+210C= NP_001135931.2:n.584+210C=
NM_001142460.1:c.584+210C= NP_001135932.2:n.584+210C=
NM_080871.3:c.539+210C= NP_543147.2:n.539+210C=
XM_005249949.3:c.719+210C= XP_005250006.1:n.719+210C=
NM_001142459.2:c.584+210C= MANE Select NP_001135931.2:n.584+210C=
NM_080871.4:c.539+210C= NP_543147.2:n.539+210C=
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