Canonical Allele Identifier: CA370035636
Gene: ASB10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151186395A>G , CM000669.2:g.151186395A>G GRCh38
NC_000007.13:g.150883482A>G , CM000669.1:g.150883482A>G GRCh37
NC_000007.12:g.150514415A>G NCBI36
NG_017016.1:g.6438T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000420175.3:c.581T>C MANE Select ENSP00000391137.2:p.Leu194Pro
ENST00000275838.5:c.581T>C ENSP00000275838.1:p.Leu194Pro
ENST00000377867.7:c.536T>C ENSP00000367098.3:p.Leu179Pro
ENST00000420175.2:c.581T>C ENSP00000391137.2:p.Leu194Pro
NM_001142459.1:c.581T>C NP_001135931.2:p.Leu194Pro
NM_001142460.1:c.581T>C NP_001135932.2:p.Leu194Pro
NM_080871.3:c.536T>C NP_543147.2:p.Leu179Pro
XM_005249949.3:c.716T>C XP_005250006.1:p.Leu239Pro
NM_001142459.2:c.581T>C MANE Select NP_001135931.2:p.Leu194Pro
NM_080871.4:c.536T>C NP_543147.2:p.Leu179Pro