Canonical Allele Identifier: CA2739944776
Gene: ASB10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187247G>T , CM000669.2:g.151187247G>T GRCh38
NC_000007.13:g.150884334G>T , CM000669.1:g.150884334G>T GRCh37
NC_000007.12:g.150515267G>T NCBI36
NG_017016.1:g.5586C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000420175.3:c.-117C>A MANE Select ENSP00000391137.2:n.-117C>A
ENST00000275838.5:c.-117C>A ENSP00000275838.1:n.-117C>A
ENST00000377867.7:c.271+205C>A ENSP00000367098.3:n.271+205C>A
ENST00000415615.1:c.*121+7C>A ENSP00000410871.1:n.*121+7C>A
NM_001142459.1:c.-117C>A NP_001135931.2:n.-117C>A
NM_001142460.1:c.-117C>A NP_001135932.2:n.-117C>A
NM_080871.3:c.271+205C>A NP_543147.2:n.271+205C>A
XM_005249949.3:c.19C>A XP_005250006.1:p.Leu7Ile
NM_001142459.2:c.-117C>A MANE Select NP_001135931.2:n.-117C>A
NM_080871.4:c.271+205C>A NP_543147.2:n.271+205C>A
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