Canonical Allele Identifier: CA2664005109
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869100_240869101insCGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGA , CM000664.2:g.240869100_240869101insCGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGA GRCh38
NC_000002.11:g.241808517_241808518insCGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGA , CM000664.1:g.241808517_241808518insCGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGA GRCh37
NC_000002.10:g.241457190_241457191insCGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGA NCBI36
NG_008005.1:g.5356_5357insCGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGA

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.166-70_166-69insCGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGA MANE Select ENSP00000302620.3:n.166-70_166-69insCGGGG...
ENST00000307503.3:c.166-70_166-69insCGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGA ENSP00000302620.3:n.166-70_166-69insCGGGG...
ENST00000472436.1:n.186-70_186-69insCGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGA
NM_000030.2:c.166-70_166-69insCGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGA NP_000021.1:n.166-70_166-69insCGGGGGTCACT...
XR_924060.1:n.405+1158_405+1159insTACAGGGGTGAGACCCAGGCCCCCCGAGTGAGGAAGCAGTGACCCCCGTCCCTCGTCCACGATCTGTGGGTGGG
NM_000030.3:c.166-70_166-69insCGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGA MANE Select NP_000021.1:n.166-70_166-69insCGGGGGTCACT...