Canonical Allele Identifier: CA835247423
Gene: ASB10 HGNC NCBI

Linked Data

dbSNP Id: rs1554478588
MyVariant Identifiers: chr7:g.150884283_150884284insGC (hg19) chr7:g.151187196_151187197insGC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187197_151187198dup , CM000669.2:g.151187197_151187198dup GRCh38
NC_000007.13:g.150884284_150884285dup , CM000669.1:g.150884284_150884285dup GRCh37
NC_000007.12:g.150515217_150515218dup NCBI36
NG_017016.1:g.5635_5636dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000420175.3:c.-68_-67dup MANE Select ENSP00000391137.2:n.-68_-67dup
ENST00000275838.5:c.-68_-67dup ENSP00000275838.1:n.-68_-67dup
ENST00000377867.7:c.271+254_271+255dup ENSP00000367098.3:n.271+254_271+255dup
ENST00000415615.1:c.*121+56_*121+57dup ENSP00000410871.1:n.*121+56_*121+57dup
NM_001142459.1:c.-68_-67dup NP_001135931.2:n.-68_-67dup
NM_001142460.1:c.-68_-67dup NP_001135932.2:n.-68_-67dup
NM_080871.3:c.271+254_271+255dup NP_543147.2:n.271+254_271+255dup
XM_005249949.3:c.68_69dup XP_005250006.1:p.Ser24AlafsTer26
NM_001142459.2:c.-68_-67dup MANE Select NP_001135931.2:n.-68_-67dup
NM_080871.4:c.271+254_271+255dup NP_543147.2:n.271+254_271+255dup
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