Canonical Allele Identifier: CA2685657602

Gene: ASB10

Linked Data

• gnomAD v4: 7-151186775-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186781_151186782del , CM000669.2:g.151186781_151186782del	GRCh38
NC_000007.13:g.150883868_150883869del , CM000669.1:g.150883868_150883869del	GRCh37
NC_000007.12:g.150514801_150514802del	NCBI36
NG_017016.1:g.6056_6057del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.316+38_316+39del MANE Select	ENSP00000391137.2:n.316+38_316+39del
ENST00000275838.5:c.316+38_316+39del	ENSP00000275838.1:n.316+38_316+39del
ENST00000377867.7:c.272-118_272-117del	ENSP00000367098.3:n.272-118_272-117del
ENST00000415615.1:c.*360+38_*360+39del	ENSP00000410871.1:n.*360+38_*360+39del
ENST00000420175.2:c.316+38_316+39del	ENSP00000391137.2:n.316+38_316+39del
NM_001142459.1:c.316+38_316+39del	NP_001135931.2:n.316+38_316+39del
NM_001142460.1:c.316+38_316+39del	NP_001135932.2:n.316+38_316+39del
NM_080871.3:c.272-118_272-117del	NP_543147.2:n.272-118_272-117del
XM_005249949.3:c.451+38_451+39del	XP_005250006.1:n.451+38_451+39del
NM_001142459.2:c.316+38_316+39del MANE Select	NP_001135931.2:n.316+38_316+39del
NM_080871.4:c.272-118_272-117del	NP_543147.2:n.272-118_272-117del