Canonical Allele Identifier: CA2685657711
Gene: ASB10 HGNC NCBI

Linked Data

gnomAD v4: 7-151187220-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187220A>G , CM000669.2:g.151187220A>G GRCh38
NC_000007.13:g.150884307A>G , CM000669.1:g.150884307A>G GRCh37
NC_000007.12:g.150515240A>G NCBI36
NG_017016.1:g.5613T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000420175.3:c.-90T>C MANE Select ENSP00000391137.2:n.-90T>C
ENST00000275838.5:c.-90T>C ENSP00000275838.1:n.-90T>C
ENST00000377867.7:c.271+232T>C ENSP00000367098.3:n.271+232T>C
ENST00000415615.1:c.*121+34T>C ENSP00000410871.1:n.*121+34T>C
NM_001142459.1:c.-90T>C NP_001135931.2:n.-90T>C
NM_001142460.1:c.-90T>C NP_001135932.2:n.-90T>C
NM_080871.3:c.271+232T>C NP_543147.2:n.271+232T>C
XM_005249949.3:c.46T>C XP_005250006.1:p.Cys16Arg
NM_001142459.2:c.-90T>C MANE Select NP_001135931.2:n.-90T>C
NM_080871.4:c.271+232T>C NP_543147.2:n.271+232T>C
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