Canonical Allele Identifier: CA4573976
Gene: ASB10 HGNC NCBI

Linked Data

dbSNP Id: rs764682358

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151186980C>T , CM000669.2:g.151186980C>T GRCh38
NC_000007.13:g.150884067C>T , CM000669.1:g.150884067C>T GRCh37
NC_000007.12:g.150515000C>T NCBI36
NG_017016.1:g.5853G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000420175.3:c.151G>A MANE Select ENSP00000391137.2:p.Ala51Thr
ENST00000275838.5:c.151G>A ENSP00000275838.1:p.Ala51Thr
ENST00000377867.7:c.272-321G>A ENSP00000367098.3:n.272-321G>A
ENST00000415615.1:c.*195G>A ENSP00000410871.1:n.*195G>A
ENST00000420175.2:c.151G>A ENSP00000391137.2:p.Ala51Thr
NM_001142459.1:c.151G>A NP_001135931.2:p.Ala51Thr
NM_001142460.1:c.151G>A NP_001135932.2:p.Ala51Thr
NM_080871.3:c.272-321G>A NP_543147.2:n.272-321G>A
XM_005249949.3:c.286G>A XP_005250006.1:p.Ala96Thr
NM_001142459.2:c.151G>A MANE Select NP_001135931.2:p.Ala51Thr
NM_080871.4:c.272-321G>A NP_543147.2:n.272-321G>A