Canonical Allele Identifier: CA4574040
Gene: ASB10 HGNC NCBI

Linked Data

dbSNP Id: rs773953818
ExAC: 7:150884399 AGGTGTAGGCTATTGG / A
gnomAD v2: 7-150884399-AGGTGTAGGCTATTGG-A
gnomAD v3: 7-151187312-AGGTGTAGGCTATTGG-A
gnomAD v4: 7-151187312-AGGTGTAGGCTATTGG-A
MyVariant Identifiers: chr7:g.150884400_150884414del (hg19) chr7:g.151187313_151187327del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187314_151187328del , CM000669.2:g.151187314_151187328del GRCh38
NC_000007.13:g.150884401_150884415del , CM000669.1:g.150884401_150884415del GRCh37
NC_000007.12:g.150515334_150515348del NCBI36
NG_017016.1:g.5506_5520del

Transcript Alleles

HGVS Amino-acid Change
ENST00000275838.5:c.-197_-183del ENSP00000275838.1:n.-197_-183del
ENST00000377867.7:c.271+125_271+139del ENSP00000367098.3:n.271+125_271+139del
ENST00000415615.1:c.*48_*62del ENSP00000410871.1:n.*48_*62del
NM_001142459.1:c.-197_-183del NP_001135931.2:n.-197_-183del
NM_001142460.1:c.-197_-183del NP_001135932.2:n.-197_-183del
NM_080871.3:c.271+125_271+139del NP_543147.2:n.271+125_271+139del
NM_080871.4:c.271+125_271+139del NP_543147.2:n.271+125_271+139del
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