Canonical Allele Identifier: CA579077294

Gene: ASB10

Linked Data

• dbSNP Id: rs1563578884
• gnomAD v2: 7-150884396-CCA-C
• gnomAD v4: 7-151187309-CCA-C
• MyVariant Identifiers: chr7:g.150884397_150884398del (hg19) ; chr7:g.151187310_151187311del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151187310_151187311del , CM000669.2:g.151187310_151187311del	GRCh38
NC_000007.13:g.150884397_150884398del , CM000669.1:g.150884397_150884398del	GRCh37
NC_000007.12:g.150515330_150515331del	NCBI36
NG_017016.1:g.5522_5523del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275838.5:c.-181_-180del	ENSP00000275838.1:n.-181_-180del
ENST00000377867.7:c.271+141_271+142del	ENSP00000367098.3:n.271+141_271+142del
ENST00000415615.1:c.*64_*65del	ENSP00000410871.1:n.*64_*65del
NM_001142459.1:c.-181_-180del	NP_001135931.2:n.-181_-180del
NM_001142460.1:c.-181_-180del	NP_001135932.2:n.-181_-180del
NM_080871.3:c.271+141_271+142del	NP_543147.2:n.271+141_271+142del
NM_080871.4:c.271+141_271+142del	NP_543147.2:n.271+141_271+142del