Canonical Allele Identifier: CA1339334168
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875117T= , CM000664.2:g.240875117T= GRCh38
NC_000002.11:g.241814534T= , CM000664.1:g.241814534T= GRCh37
NC_000002.10:g.241463207T= NCBI36
NG_008005.1:g.11373T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.689T= MANE Select ENSP00000302620.3:p.Met230=
ENST00000307503.3:c.689T= ENSP00000302620.3:p.Met230=
ENST00000476698.1:n.341T=
NM_000030.2:c.689T= NP_000021.1:p.Met230=
NM_000030.3:c.689T= MANE Select NP_000021.1:p.Met230=
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