Canonical Allele Identifier: CA1752544665

Gene: ASB10

Linked Data

• dbSNP Id: rs1801587885
• gnomAD v4: 7-151186312-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186316del , CM000669.2:g.151186316del	GRCh38
NC_000007.13:g.150883403del , CM000669.1:g.150883403del	GRCh37
NC_000007.12:g.150514336del	NCBI36
NG_017016.1:g.6520del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.584+79del MANE Select	ENSP00000391137.2:n.584+79del
ENST00000275838.5:c.584+79del	ENSP00000275838.1:n.584+79del
ENST00000377867.7:c.539+79del	ENSP00000367098.3:n.539+79del
ENST00000420175.2:c.584+79del	ENSP00000391137.2:n.584+79del
NM_001142459.1:c.584+79del	NP_001135931.2:n.584+79del
NM_001142460.1:c.584+79del	NP_001135932.2:n.584+79del
NM_080871.3:c.539+79del	NP_543147.2:n.539+79del
XM_005249949.3:c.719+79del	XP_005250006.1:n.719+79del
NM_001142459.2:c.584+79del MANE Select	NP_001135931.2:n.584+79del
NM_080871.4:c.539+79del	NP_543147.2:n.539+79del