Canonical Allele Identifier: CA2664005384
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869114_240869115insCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCT , CM000664.2:g.240869114_240869115insCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCT GRCh38
NC_000002.11:g.241808531_241808532insCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCT , CM000664.1:g.241808531_241808532insCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCT GRCh37
NC_000002.10:g.241457204_241457205insCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCT NCBI36
NG_008005.1:g.5370_5371insCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCT

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.166-56_166-55insCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCT MANE Select ENSP00000302620.3:n.166-56_166-55insCTCAC...
ENST00000307503.3:c.166-56_166-55insCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCT ENSP00000302620.3:n.166-56_166-55insCTCAC...
ENST00000472436.1:n.186-56_186-55insCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCT
NM_000030.2:c.166-56_166-55insCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCT NP_000021.1:n.166-56_166-55insCTCACTCGGGG...
XR_924060.1:n.405+1118_405+1119insAGCAGTGACCCCCTTCCCTCGTCCACGATCTGTGGGTGGGTACAGGGGTGAGACCCAGGCCCCCCGAGTGAG
NM_000030.3:c.166-56_166-55insCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCT MANE Select NP_000021.1:n.166-56_166-55insCTCACTCGGGG...