Canonical Allele Identifier: CA2685657483
Gene: ASB10 HGNC NCBI

Linked Data

gnomAD v4: 7-151186363-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151186363A>G , CM000669.2:g.151186363A>G GRCh38
NC_000007.13:g.150883450A>G , CM000669.1:g.150883450A>G GRCh37
NC_000007.12:g.150514383A>G NCBI36
NG_017016.1:g.6470T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000420175.3:c.584+29T>C MANE Select ENSP00000391137.2:n.584+29T>C
ENST00000275838.5:c.584+29T>C ENSP00000275838.1:n.584+29T>C
ENST00000377867.7:c.539+29T>C ENSP00000367098.3:n.539+29T>C
ENST00000420175.2:c.584+29T>C ENSP00000391137.2:n.584+29T>C
NM_001142459.1:c.584+29T>C NP_001135931.2:n.584+29T>C
NM_001142460.1:c.584+29T>C NP_001135932.2:n.584+29T>C
NM_080871.3:c.539+29T>C NP_543147.2:n.539+29T>C
XM_005249949.3:c.719+29T>C XP_005250006.1:n.719+29T>C
NM_001142459.2:c.584+29T>C MANE Select NP_001135931.2:n.584+29T>C
NM_080871.4:c.539+29T>C NP_543147.2:n.539+29T>C
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