Canonical Allele Identifier: CA1752545549

Gene: ASB10

Linked Data

• dbSNP Id: rs1801604599

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186801_151186802insA , CM000669.2:g.151186801_151186802insA	GRCh38
NC_000007.13:g.150883888_150883889insA , CM000669.1:g.150883888_150883889insA	GRCh37
NC_000007.12:g.150514821_150514822insA	NCBI36
NG_017016.1:g.6031_6032insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.316+13_316+14insT MANE Select	ENSP00000391137.2:n.316+13_316+14insT
ENST00000275838.5:c.316+13_316+14insT	ENSP00000275838.1:n.316+13_316+14insT
ENST00000377867.7:c.272-143_272-142insT	ENSP00000367098.3:n.272-143_272-142insT
ENST00000415615.1:c.*360+13_*360+14insT	ENSP00000410871.1:n.*360+13_*360+14insT
ENST00000420175.2:c.316+13_316+14insT	ENSP00000391137.2:n.316+13_316+14insT
NM_001142459.1:c.316+13_316+14insT	NP_001135931.2:n.316+13_316+14insT
NM_001142460.1:c.316+13_316+14insT	NP_001135932.2:n.316+13_316+14insT
NM_080871.3:c.272-143_272-142insT	NP_543147.2:n.272-143_272-142insT
XM_005249949.3:c.451+13_451+14insT	XP_005250006.1:n.451+13_451+14insT
NM_001142459.2:c.316+13_316+14insT MANE Select	NP_001135931.2:n.316+13_316+14insT
NM_080871.4:c.272-143_272-142insT	NP_543147.2:n.272-143_272-142insT