Canonical Allele Identifier: CA1339336224
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878918_240878919delinsTG , CM000664.2:g.240878918_240878919delinsTG GRCh38
NC_000002.11:g.241818335_241818336delinsTG , CM000664.1:g.241818335_241818336delinsTG GRCh37
NC_000002.10:g.241467008_241467009delinsTG NCBI36
NG_008005.1:g.15174_15175delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*97_*98delinsTG MANE Select ENSP00000302620.3:n.*97_*98delinsTG
ENST00000307503.3:c.*97_*98delinsTG ENSP00000302620.3:n.*97_*98delinsTG
ENST00000470255.1:n.1054_1055delinsTG
NM_000030.2:c.*97_*98delinsTG NP_000021.1:n.*97_*98delinsTG
NM_000030.3:c.*97_*98delinsTG MANE Select NP_000021.1:n.*97_*98delinsTG