Canonical Allele Identifier: CA1752546476
Gene: ASB10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187361G= , CM000669.2:g.151187361G= GRCh38
NC_000007.13:g.150884448G= , CM000669.1:g.150884448G= GRCh37
NC_000007.12:g.150515381G= NCBI36
NG_017016.1:g.5472C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000275838.5:c.-231C= ENSP00000275838.1:n.-231C=
ENST00000377867.7:c.271+91C= ENSP00000367098.3:n.271+91C=
ENST00000415615.1:c.*14C= ENSP00000410871.1:n.*14C=
NM_001142459.1:c.-231C= NP_001135931.2:n.-231C=
NM_001142460.1:c.-231C= NP_001135932.2:n.-231C=
NM_080871.3:c.271+91C= NP_543147.2:n.271+91C=
NM_080871.4:c.271+91C= NP_543147.2:n.271+91C=