Canonical Allele Identifier: CA370037734
Gene: ASB10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151186986G>T , CM000669.2:g.151186986G>T GRCh38
NC_000007.13:g.150884073G>T , CM000669.1:g.150884073G>T GRCh37
NC_000007.12:g.150515006G>T NCBI36
NG_017016.1:g.5847C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000420175.3:c.145C>A MANE Select ENSP00000391137.2:p.Arg49Ser
ENST00000275838.5:c.145C>A ENSP00000275838.1:p.Arg49Ser
ENST00000377867.7:c.272-327C>A ENSP00000367098.3:n.272-327C>A
ENST00000415615.1:c.*189C>A ENSP00000410871.1:n.*189C>A
ENST00000420175.2:c.145C>A ENSP00000391137.2:p.Arg49Ser
NM_001142459.1:c.145C>A NP_001135931.2:p.Arg49Ser
NM_001142460.1:c.145C>A NP_001135932.2:p.Arg49Ser
NM_080871.3:c.272-327C>A NP_543147.2:n.272-327C>A
XM_005249949.3:c.280C>A XP_005250006.1:p.Arg94Ser
NM_001142459.2:c.145C>A MANE Select NP_001135931.2:p.Arg49Ser
NM_080871.4:c.272-327C>A NP_543147.2:n.272-327C>A