Canonical Allele Identifier: CA2664004883
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869045_240869046insGCTCGGGGGTCCTGGGTCTCACCCATGTTCCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTC , CM000664.2:g.240869045_240869046insGCTCGGGGGTCCTGGGTCTCACCCATGTTCCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTC GRCh38
NC_000002.11:g.241808462_241808463insGCTCGGGGGTCCTGGGTCTCACCCATGTTCCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTC , CM000664.1:g.241808462_241808463insGCTCGGGGGTCCTGGGTCTCACCCATGTTCCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTC GRCh37
NC_000002.10:g.241457135_241457136insGCTCGGGGGTCCTGGGTCTCACCCATGTTCCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTC NCBI36
NG_008005.1:g.5301_5302insGCTCGGGGGTCCTGGGTCTCACCCATGTTCCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTC

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.165+15_165+16insGCTCGGGGGTCCTGGGTCTCACCCATGTTCCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTC MANE Select ENSP00000302620.3:n.165+15_165+16insGCTCG...
ENST00000307503.3:c.165+15_165+16insGCTCGGGGGTCCTGGGTCTCACCCATGTTCCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTC ENSP00000302620.3:n.165+15_165+16insGCTCG...
ENST00000472436.1:n.185+15_185+16insGCTCGGGGGTCCTGGGTCTCACCCATGTTCCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTC
NM_000030.2:c.165+15_165+16insGCTCGGGGGTCCTGGGTCTCACCCATGTTCCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTC NP_000021.1:n.165+15_165+16insGCTCGGGGGTC...
XR_924060.1:n.405+1189_405+1190insGGAAGCAGTGACCCCCTTCCCTCGTCCACGATCTGTGGGTGGGAACATGGGTGAGACCCAGGACCCCCGAGCGA
NM_000030.3:c.165+15_165+16insGCTCGGGGGTCCTGGGTCTCACCCATGTTCCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTC MANE Select NP_000021.1:n.165+15_165+16insGCTCGGGGGTC...