Canonical Allele Identifier: CA2754891901
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869113_240869114insTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGCCGAGGGAAGGGGGTCAGTGC , CM000664.2:g.240869113_240869114insTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGCCGAGGGAAGGGGGTCAGTGC GRCh38
NC_000002.11:g.241808530_241808531insTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGCCGAGGGAAGGGGGTCAGTGC , CM000664.1:g.241808530_241808531insTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGCCGAGGGAAGGGGGTCAGTGC GRCh37
NC_000002.10:g.241457203_241457204insTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGCCGAGGGAAGGGGGTCAGTGC NCBI36
NG_008005.1:g.5369_5370insTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGCCGAGGGAAGGGGGTCAGTGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.166-57_166-56insTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGCCGAGGGAAGGGGGTCAGTGC MANE Select ENSP00000302620.3:n.166-57_166-56insTTCCTCACTCGGGGGGCCTGGGTCT...
ENST00000307503.3:c.166-57_166-56insTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGCCGAGGGAAGGGGGTCAGTGC ENSP00000302620.3:n.166-57_166-56insTTCCTCACTCGGGGGGCCTGGGTCT...
ENST00000472436.1:n.186-57_186-56insTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGCCGAGGGAAGGGGGTCAGTGC
NM_000030.2:c.166-57_166-56insTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGCCGAGGGAAGGGGGTCAGTGC NP_000021.1:n.166-57_166-56insTTCCTCACTCGGGGGGCCTGGGTCTCACCCC...
XR_924060.1:n.405+1122_405+1123insCTGACCCCCTTCCCTCGGCCACGATCTGTGGGTGGGTACAGGGGTGAGACCCAGGCCCCCCGAGTGAGGAAGCA
NM_000030.3:c.166-57_166-56insTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGCCGAGGGAAGGGGGTCAGTGC MANE Select NP_000021.1:n.166-57_166-56insTTCCTCACTCGGGGGGCCTGGGTCTCACCCC...