Canonical Allele Identifier: CA1339334249
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875257_240875258delinsTG , CM000664.2:g.240875257_240875258delinsTG GRCh38
NC_000002.11:g.241814674_241814675delinsTG , CM000664.1:g.241814674_241814675delinsTG GRCh37
NC_000002.10:g.241463347_241463348delinsTG NCBI36
NG_008005.1:g.11513_11514delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.776+53_776+54delinsTG MANE Select ENSP00000302620.3:n.776+53_776+54delinsTG
ENST00000307503.3:c.776+53_776+54delinsTG ENSP00000302620.3:n.776+53_776+54delinsTG
ENST00000476698.1:n.428+53_428+54delinsTG
NM_000030.2:c.776+53_776+54delinsTG NP_000021.1:n.776+53_776+54delinsTG
NM_000030.3:c.776+53_776+54delinsTG MANE Select NP_000021.1:n.776+53_776+54delinsTG