Canonical Allele Identifier: CA2739944781
Gene: ASB10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187252A>C , CM000669.2:g.151187252A>C GRCh38
NC_000007.13:g.150884339A>C , CM000669.1:g.150884339A>C GRCh37
NC_000007.12:g.150515272A>C NCBI36
NG_017016.1:g.5581T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000275838.5:c.-122T>G ENSP00000275838.1:n.-122T>G
ENST00000377867.7:c.271+200T>G ENSP00000367098.3:n.271+200T>G
ENST00000415615.1:c.*121+2T>G ENSP00000410871.1:n.*121+2T>G
NM_001142459.1:c.-122T>G NP_001135931.2:n.-122T>G
NM_001142460.1:c.-122T>G NP_001135932.2:n.-122T>G
NM_080871.3:c.271+200T>G NP_543147.2:n.271+200T>G
XM_005249949.3:c.14T>G XP_005250006.1:p.Val5Gly
NM_080871.4:c.271+200T>G NP_543147.2:n.271+200T>G