Canonical Allele Identifier: CA1339333255
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873371C= , CM000664.2:g.240873371C= GRCh38
NC_000002.11:g.241812788C= , CM000664.1:g.241812788C= GRCh37
NC_000002.10:g.241461461C= NCBI36
NG_008005.1:g.9627C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.595+322C= MANE Select ENSP00000302620.3:n.595+322C=
ENST00000307503.3:c.595+322C= ENSP00000302620.3:n.595+322C=
ENST00000472436.1:n.937C=
ENST00000476698.1:n.332+322C=
NM_000030.2:c.595+322C= NP_000021.1:n.595+322C=
NM_000030.3:c.595+322C= MANE Select NP_000021.1:n.595+322C=
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