Canonical Allele Identifier: CA1339336135
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878745C= , CM000664.2:g.240878745C= GRCh38
NC_000002.11:g.241818162C= , CM000664.1:g.241818162C= GRCh37
NC_000002.10:g.241466835C= NCBI36
NG_008005.1:g.15001C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.1103C= MANE Select ENSP00000302620.3:p.Ala368=
ENST00000307503.3:c.1103C= ENSP00000302620.3:p.Ala368=
ENST00000470255.1:n.881C=
NM_000030.2:c.1103C= NP_000021.1:p.Ala368=
NM_000030.3:c.1103C= MANE Select NP_000021.1:p.Ala368=
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