Canonical Allele Identifier: CA2685657513
Gene: ASB10 HGNC NCBI

Linked Data

gnomAD v4: 7-151186389-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151186389C>T , CM000669.2:g.151186389C>T GRCh38
NC_000007.13:g.150883476C>T , CM000669.1:g.150883476C>T GRCh37
NC_000007.12:g.150514409C>T NCBI36
NG_017016.1:g.6444G>A

Transcript Alleles

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