Canonical Allele Identifier: CA1752544688
Gene: ASB10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151186326T= , CM000669.2:g.151186326T= GRCh38
NC_000007.13:g.150883413T= , CM000669.1:g.150883413T= GRCh37
NC_000007.12:g.150514346T= NCBI36
NG_017016.1:g.6507A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000420175.3:c.584+66A= MANE Select ENSP00000391137.2:n.584+66A=
ENST00000275838.5:c.584+66A= ENSP00000275838.1:n.584+66A=
ENST00000377867.7:c.539+66A= ENSP00000367098.3:n.539+66A=
ENST00000420175.2:c.584+66A= ENSP00000391137.2:n.584+66A=
NM_001142459.1:c.584+66A= NP_001135931.2:n.584+66A=
NM_001142460.1:c.584+66A= NP_001135932.2:n.584+66A=
NM_080871.3:c.539+66A= NP_543147.2:n.539+66A=
XM_005249949.3:c.719+66A= XP_005250006.1:n.719+66A=
NM_001142459.2:c.584+66A= MANE Select NP_001135931.2:n.584+66A=
NM_080871.4:c.539+66A= NP_543147.2:n.539+66A=
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