Canonical Allele Identifier: CA2664005091
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869078_240869079insACCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCA , CM000664.2:g.240869078_240869079insACCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCA GRCh38
NC_000002.11:g.241808495_241808496insACCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCA , CM000664.1:g.241808495_241808496insACCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCA GRCh37
NC_000002.10:g.241457168_241457169insACCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCA NCBI36
NG_008005.1:g.5334_5335insACCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCA

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.165+48_165+49insACCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCA MANE Select ENSP00000302620.3:n.165+48_165+49insACCAC...
ENST00000307503.3:c.165+48_165+49insACCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCA ENSP00000302620.3:n.165+48_165+49insACCAC...
ENST00000472436.1:n.185+48_185+49insACCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCA
NM_000030.2:c.165+48_165+49insACCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCA NP_000021.1:n.165+48_165+49insACCACAGATCG...
XR_924060.1:n.405+1158_405+1159insTACAGGGGTGAGACCCAGGCCCCCCGAGTGAGGAAGCAGTGACCCCCTTCCCTCGTCCACGATCTGTGGTTGGG
NM_000030.3:c.165+48_165+49insACCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCA MANE Select NP_000021.1:n.165+48_165+49insACCACAGATCG...