Canonical Allele Identifier: CA1752545730

Gene: ASB10

Linked Data

• dbSNP Id: rs1801610184

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186964del , CM000669.2:g.151186964del	GRCh38
NC_000007.13:g.150884051del , CM000669.1:g.150884051del	GRCh37
NC_000007.12:g.150514984del	NCBI36
NG_017016.1:g.5870del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.168del MANE Select	ENSP00000391137.2:p.Ala57ProfsTer?
ENST00000275838.5:c.168del	ENSP00000275838.1:p.Ala57ProfsTer?
ENST00000377867.7:c.272-304del	ENSP00000367098.3:n.272-304del
ENST00000415615.1:c.*212del	ENSP00000410871.1:n.*212del
ENST00000420175.2:c.168del	ENSP00000391137.2:p.Ala57ProfsTer?
NM_001142459.1:c.168del	NP_001135931.2:p.Ala57ProfsTer?
NM_001142460.1:c.168del	NP_001135932.2:p.Ala57ProfsTer?
NM_080871.3:c.272-304del	NP_543147.2:n.272-304del
XM_005249949.3:c.303del	XP_005250006.1:p.Ala102ProfsTer?
NM_001142459.2:c.168del MANE Select	NP_001135931.2:p.Ala57ProfsTer?
NM_080871.4:c.272-304del	NP_543147.2:n.272-304del