Canonical Allele Identifier: CA1339334202
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875179_240875180delinsTG , CM000664.2:g.240875179_240875180delinsTG GRCh38
NC_000002.11:g.241814596_241814597delinsTG , CM000664.1:g.241814596_241814597delinsTG GRCh37
NC_000002.10:g.241463269_241463270delinsTG NCBI36
NG_008005.1:g.11435_11436delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.751_752delinsTG MANE Select ENSP00000302620.3:p.Trp251=
ENST00000307503.3:c.751_752delinsTG ENSP00000302620.3:p.Trp251=
ENST00000476698.1:n.403_404delinsTG
NM_000030.2:c.751_752delinsTG NP_000021.1:p.Trp251=
NM_000030.3:c.751_752delinsTG MANE Select NP_000021.1:p.Trp251=
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