Canonical Allele Identifier: CA1339335540
Gene: AGXT HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877608_240877609delinsGC , CM000664.2:g.240877608_240877609delinsGC GRCh38
NC_000002.11:g.241817025_241817026delinsGC , CM000664.1:g.241817025_241817026delinsGC GRCh37
NC_000002.10:g.241465698_241465699delinsGC NCBI36
NG_008005.1:g.13864_13865delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.918_919delinsGC MANE Select ENSP00000302620.3:p.Gly306=
ENST00000307503.3:c.918_919delinsGC ENSP00000302620.3:p.Gly306=
ENST00000470255.1:n.696_697delinsGC
NM_000030.2:c.918_919delinsGC NP_000021.1:p.Gly306=
NM_000030.3:c.918_919delinsGC MANE Select NP_000021.1:p.Gly306=
Search 100 bp 5'
Search 100 bp 3'