Canonical Allele Identifier: CA2739944793
Gene: ASB10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187262G>C , CM000669.2:g.151187262G>C GRCh38
NC_000007.13:g.150884349G>C , CM000669.1:g.150884349G>C GRCh37
NC_000007.12:g.150515282G>C NCBI36
NG_017016.1:g.5571C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000275838.5:c.-132C>G ENSP00000275838.1:n.-132C>G
ENST00000377867.7:c.271+190C>G ENSP00000367098.3:n.271+190C>G
ENST00000415615.1:c.*113C>G ENSP00000410871.1:n.*113C>G
NM_001142459.1:c.-132C>G NP_001135931.2:n.-132C>G
NM_001142460.1:c.-132C>G NP_001135932.2:n.-132C>G
NM_080871.3:c.271+190C>G NP_543147.2:n.271+190C>G
XM_005249949.3:c.4C>G XP_005250006.1:p.Arg2Gly
NM_080871.4:c.271+190C>G NP_543147.2:n.271+190C>G