Canonical Allele Identifier: CA579077280

Gene: ASB10

Linked Data

• dbSNP Id: rs1202158905
• gnomAD v2: 7-150884286-AG-A
• gnomAD v4: 7-151187199-AG-A
• MyVariant Identifiers: chr7:g.150884287del (hg19) ; chr7:g.151187200del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187201del , CM000669.2:g.151187201del	GRCh38
NC_000007.13:g.150884288del , CM000669.1:g.150884288del	GRCh37
NC_000007.12:g.150515221del	NCBI36
NG_017016.1:g.5633del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420175.3:c.-70del MANE Select	ENSP00000391137.2:n.-70del
ENST00000275838.5:c.-70del	ENSP00000275838.1:n.-70del
ENST00000377867.7:c.271+252del	ENSP00000367098.3:n.271+252del
ENST00000415615.1:c.*121+54del	ENSP00000410871.1:n.*121+54del
NM_001142459.1:c.-70del	NP_001135931.2:n.-70del
NM_001142460.1:c.-70del	NP_001135932.2:n.-70del
NM_080871.3:c.271+252del	NP_543147.2:n.271+252del
XM_005249949.3:c.66del	XP_005250006.1:p.Cys23AlafsTer26
NM_001142459.2:c.-70del MANE Select	NP_001135931.2:n.-70del
NM_080871.4:c.271+252del	NP_543147.2:n.271+252del