Canonical Allele Identifier: CA1752545902
Gene: ASB10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151187087_151187088delinsTC , CM000669.2:g.151187087_151187088delinsTC GRCh38
NC_000007.13:g.150884174_150884175delinsTC , CM000669.1:g.150884174_150884175delinsTC GRCh37
NC_000007.12:g.150515107_150515108delinsTC NCBI36
NG_017016.1:g.5745_5746delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000420175.3:c.43_44delinsGA MANE Select ENSP00000391137.2:p.Glu15=
ENST00000275838.5:c.43_44delinsGA ENSP00000275838.1:p.Glu15=
ENST00000377867.7:c.271+364_271+365delinsGA ENSP00000367098.3:n.271+364_271+365delinsGA
ENST00000415615.1:c.*122-35_*122-34delinsGA ENSP00000410871.1:n.*122-35_*122-34delinsGA
ENST00000420175.2:c.43_44delinsGA ENSP00000391137.2:p.Glu15=
NM_001142459.1:c.43_44delinsGA NP_001135931.2:p.Glu15=
NM_001142460.1:c.43_44delinsGA NP_001135932.2:p.Glu15=
NM_080871.3:c.271+364_271+365delinsGA NP_543147.2:n.271+364_271+365delinsGA
XM_005249949.3:c.178_179delinsGA XP_005250006.1:p.Glu60=
NM_001142459.2:c.43_44delinsGA MANE Select NP_001135931.2:p.Glu15=
NM_080871.4:c.271+364_271+365delinsGA NP_543147.2:n.271+364_271+365delinsGA