Canonical Allele Identifier: CA1339332083
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240871367C= , CM000664.2:g.240871367C= GRCh38
NC_000002.11:g.241810784C= , CM000664.1:g.241810784C= GRCh37
NC_000002.10:g.241459457C= NCBI36
NG_008005.1:g.7623C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.442C= MANE Select ENSP00000302620.3:p.Pro148=
ENST00000307503.3:c.442C= ENSP00000302620.3:p.Pro148=
ENST00000472436.1:n.462C=
ENST00000476698.1:n.179C=
NM_000030.2:c.442C= NP_000021.1:p.Pro148=
NM_000030.3:c.442C= MANE Select NP_000021.1:p.Pro148=
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