Canonical Allele Identifier: CA2685657611

Gene: ASB10

Linked Data

• gnomAD v4: 7-151186792-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151186797del , CM000669.2:g.151186797del	GRCh38
NC_000007.13:g.150883884del , CM000669.1:g.150883884del	GRCh37
NC_000007.12:g.150514817del	NCBI36
NG_017016.1:g.6040del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.316+22del MANE Select	ENSP00000391137.2:n.316+22del
ENST00000275838.5:c.316+22del	ENSP00000275838.1:n.316+22del
ENST00000377867.7:c.272-134del	ENSP00000367098.3:n.272-134del
ENST00000415615.1:c.*360+22del	ENSP00000410871.1:n.*360+22del
ENST00000420175.2:c.316+22del	ENSP00000391137.2:n.316+22del
NM_001142459.1:c.316+22del	NP_001135931.2:n.316+22del
NM_001142460.1:c.316+22del	NP_001135932.2:n.316+22del
NM_080871.3:c.272-134del	NP_543147.2:n.272-134del
XM_005249949.3:c.451+22del	XP_005250006.1:n.451+22del
NM_001142459.2:c.316+22del MANE Select	NP_001135931.2:n.316+22del
NM_080871.4:c.272-134del	NP_543147.2:n.272-134del