Canonical Allele Identifier: CA1339334669
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875999G= , CM000664.2:g.240875999G= GRCh38
NC_000002.11:g.241815416G= , CM000664.1:g.241815416G= GRCh37
NC_000002.10:g.241464089G= NCBI36
NG_008005.1:g.12255G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.841G= MANE Select ENSP00000302620.3:p.Glu281=
ENST00000307503.3:c.841G= ENSP00000302620.3:p.Glu281=
ENST00000476698.1:n.493G=
NM_000030.2:c.841G= NP_000021.1:p.Glu281=
NM_000030.3:c.841G= MANE Select NP_000021.1:p.Glu281=
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