Canonical Allele Identifier: CA2739944744
Gene: ASB10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187228C>T , CM000669.2:g.151187228C>T GRCh38
NC_000007.13:g.150884315C>T , CM000669.1:g.150884315C>T GRCh37
NC_000007.12:g.150515248C>T NCBI36
NG_017016.1:g.5605G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000420175.3:c.-98G>A MANE Select ENSP00000391137.2:n.-98G>A
ENST00000275838.5:c.-98G>A ENSP00000275838.1:n.-98G>A
ENST00000377867.7:c.271+224G>A ENSP00000367098.3:n.271+224G>A
ENST00000415615.1:c.*121+26G>A ENSP00000410871.1:n.*121+26G>A
NM_001142459.1:c.-98G>A NP_001135931.2:n.-98G>A
NM_001142460.1:c.-98G>A NP_001135932.2:n.-98G>A
NM_080871.3:c.271+224G>A NP_543147.2:n.271+224G>A
XM_005249949.3:c.38G>A XP_005250006.1:p.Gly13Glu
NM_001142459.2:c.-98G>A MANE Select NP_001135931.2:n.-98G>A
NM_080871.4:c.271+224G>A NP_543147.2:n.271+224G>A