Canonical Allele Identifier: CA2685657775

Gene: ASB10

Linked Data

• gnomAD v4: 7-151187356-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187361del , CM000669.2:g.151187361del	GRCh38
NC_000007.13:g.150884448del , CM000669.1:g.150884448del	GRCh37
NC_000007.12:g.150515381del	NCBI36
NG_017016.1:g.5476del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275838.5:c.-227del	ENSP00000275838.1:n.-227del
ENST00000377867.7:c.271+95del	ENSP00000367098.3:n.271+95del
ENST00000415615.1:c.*18del	ENSP00000410871.1:n.*18del
NM_001142459.1:c.-227del	NP_001135931.2:n.-227del
NM_001142460.1:c.-227del	NP_001135932.2:n.-227del
NM_080871.3:c.271+95del	NP_543147.2:n.271+95del
NM_080871.4:c.271+95del	NP_543147.2:n.271+95del