Canonical Allele Identifier: CA1752544730

Gene: ASB10

Linked Data

• dbSNP Id: rs1801589893

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186375_151186376del , CM000669.2:g.151186375_151186376del	GRCh38
NC_000007.13:g.150883462_150883463del , CM000669.1:g.150883462_150883463del	GRCh37
NC_000007.12:g.150514395_150514396del	NCBI36
NG_017016.1:g.6459_6460del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.584+18_584+19del MANE Select	ENSP00000391137.2:n.584+18_584+19del
ENST00000275838.5:c.584+18_584+19del	ENSP00000275838.1:n.584+18_584+19del
ENST00000377867.7:c.539+18_539+19del	ENSP00000367098.3:n.539+18_539+19del
ENST00000420175.2:c.584+18_584+19del	ENSP00000391137.2:n.584+18_584+19del
NM_001142459.1:c.584+18_584+19del	NP_001135931.2:n.584+18_584+19del
NM_001142460.1:c.584+18_584+19del	NP_001135932.2:n.584+18_584+19del
NM_080871.3:c.539+18_539+19del	NP_543147.2:n.539+18_539+19del
XM_005249949.3:c.719+18_719+19del	XP_005250006.1:n.719+18_719+19del
NM_001142459.2:c.584+18_584+19del MANE Select	NP_001135931.2:n.584+18_584+19del
NM_080871.4:c.539+18_539+19del	NP_543147.2:n.539+18_539+19del