Canonical Allele Identifier: CA2685657706

Gene: ASB10

Linked Data

• gnomAD v4: 7-151187215-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187216del , CM000669.2:g.151187216del	GRCh38
NC_000007.13:g.150884303del , CM000669.1:g.150884303del	GRCh37
NC_000007.12:g.150515236del	NCBI36
NG_017016.1:g.5617del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.-86del MANE Select	ENSP00000391137.2:n.-86del
ENST00000275838.5:c.-86del	ENSP00000275838.1:n.-86del
ENST00000377867.7:c.271+236del	ENSP00000367098.3:n.271+236del
ENST00000415615.1:c.*121+38del	ENSP00000410871.1:n.*121+38del
NM_001142459.1:c.-86del	NP_001135931.2:n.-86del
NM_001142460.1:c.-86del	NP_001135932.2:n.-86del
NM_080871.3:c.271+236del	NP_543147.2:n.271+236del
XM_005249949.3:c.50del	XP_005250006.1:p.Leu17ArgfsTer?
NM_001142459.2:c.-86del MANE Select	NP_001135931.2:n.-86del
NM_080871.4:c.271+236del	NP_543147.2:n.271+236del