Canonical Allele Identifier: CA2685657701

Gene: ASB10

Linked Data

• gnomAD v4: 7-151187211-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187212del , CM000669.2:g.151187212del	GRCh38
NC_000007.13:g.150884299del , CM000669.1:g.150884299del	GRCh37
NC_000007.12:g.150515232del	NCBI36
NG_017016.1:g.5621del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.-82del MANE Select	ENSP00000391137.2:n.-82del
ENST00000275838.5:c.-82del	ENSP00000275838.1:n.-82del
ENST00000377867.7:c.271+240del	ENSP00000367098.3:n.271+240del
ENST00000415615.1:c.*121+42del	ENSP00000410871.1:n.*121+42del
NM_001142459.1:c.-82del	NP_001135931.2:n.-82del
NM_001142460.1:c.-82del	NP_001135932.2:n.-82del
NM_080871.3:c.271+240del	NP_543147.2:n.271+240del
XM_005249949.3:c.54del	XP_005250006.1:p.Val19TyrfsTer?
NM_001142459.2:c.-82del MANE Select	NP_001135931.2:n.-82del
NM_080871.4:c.271+240del	NP_543147.2:n.271+240del