Canonical Allele Identifier: CA2664005052
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869113_240869114insTTCCTCACTCGGGGGGCCTGGGTCTCACCTCTGTACCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGC , CM000664.2:g.240869113_240869114insTTCCTCACTCGGGGGGCCTGGGTCTCACCTCTGTACCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGC GRCh38
NC_000002.11:g.241808530_241808531insTTCCTCACTCGGGGGGCCTGGGTCTCACCTCTGTACCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGC , CM000664.1:g.241808530_241808531insTTCCTCACTCGGGGGGCCTGGGTCTCACCTCTGTACCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGC GRCh37
NC_000002.10:g.241457203_241457204insTTCCTCACTCGGGGGGCCTGGGTCTCACCTCTGTACCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGC NCBI36
NG_008005.1:g.5369_5370insTTCCTCACTCGGGGGGCCTGGGTCTCACCTCTGTACCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.166-57_166-56insTTCCTCACTCGGGGGGCCTGGGTCTCACCTCTGTACCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGC MANE Select ENSP00000302620.3:n.166-57_166-56insTTCCTCACTCGGGGGGCCTGGGTCT...
ENST00000307503.3:c.166-57_166-56insTTCCTCACTCGGGGGGCCTGGGTCTCACCTCTGTACCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGC ENSP00000302620.3:n.166-57_166-56insTTCCTCACTCGGGGGGCCTGGGTCT...
ENST00000472436.1:n.186-57_186-56insTTCCTCACTCGGGGGGCCTGGGTCTCACCTCTGTACCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGC
NM_000030.2:c.166-57_166-56insTTCCTCACTCGGGGGGCCTGGGTCTCACCTCTGTACCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGC NP_000021.1:n.166-57_166-56insTTCCTCACTCGGGGGGCCTGGGTCTCACCTC...
XR_924060.1:n.405+1158_405+1159insTACAGAGGTGAGACCCAGGCCCCCCGAGTGAGGAAGCAGTGACCCCCTTCCCTCGTCCACGATCTGTGGGTGGG
NM_000030.3:c.166-57_166-56insTTCCTCACTCGGGGGGCCTGGGTCTCACCTCTGTACCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGC MANE Select NP_000021.1:n.166-57_166-56insTTCCTCACTCGGGGGGCCTGGGTCTCACCTC...