Canonical Allele Identifier: CA370036723
Gene: ASB10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151186817A>G , CM000669.2:g.151186817A>G GRCh38
NC_000007.13:g.150883904A>G , CM000669.1:g.150883904A>G GRCh37
NC_000007.12:g.150514837A>G NCBI36
NG_017016.1:g.6016T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000420175.3:c.314T>C MANE Select ENSP00000391137.2:p.Leu105Pro
ENST00000275838.5:c.314T>C ENSP00000275838.1:p.Leu105Pro
ENST00000377867.7:c.272-158T>C ENSP00000367098.3:n.272-158T>C
ENST00000415615.1:c.*358T>C ENSP00000410871.1:n.*358T>C
ENST00000420175.2:c.314T>C ENSP00000391137.2:p.Leu105Pro
NM_001142459.1:c.314T>C NP_001135931.2:p.Leu105Pro
NM_001142460.1:c.314T>C NP_001135932.2:p.Leu105Pro
NM_080871.3:c.272-158T>C NP_543147.2:n.272-158T>C
XM_005249949.3:c.449T>C XP_005250006.1:p.Leu150Pro
NM_001142459.2:c.314T>C MANE Select NP_001135931.2:p.Leu105Pro
NM_080871.4:c.272-158T>C NP_543147.2:n.272-158T>C