Canonical Allele Identifier: CA2685657743

Gene: ASB10

Linked Data

• gnomAD v4: 7-151187291-CAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187292_151187293del , CM000669.2:g.151187292_151187293del	GRCh38
NC_000007.13:g.150884379_150884380del , CM000669.1:g.150884379_150884380del	GRCh37
NC_000007.12:g.150515312_150515313del	NCBI36
NG_017016.1:g.5540_5541del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275838.5:c.-163_-162del	ENSP00000275838.1:n.-163_-162del
ENST00000377867.7:c.271+159_271+160del	ENSP00000367098.3:n.271+159_271+160del
ENST00000415615.1:c.*82_*83del	ENSP00000410871.1:n.*82_*83del
NM_001142459.1:c.-163_-162del	NP_001135931.2:n.-163_-162del
NM_001142460.1:c.-163_-162del	NP_001135932.2:n.-163_-162del
NM_080871.3:c.271+159_271+160del	NP_543147.2:n.271+159_271+160del
NM_080871.4:c.271+159_271+160del	NP_543147.2:n.271+159_271+160del