Canonical Allele Identifier: CA1339334189
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875156A= , CM000664.2:g.240875156A= GRCh38
NC_000002.11:g.241814573A= , CM000664.1:g.241814573A= GRCh37
NC_000002.10:g.241463246A= NCBI36
NG_008005.1:g.11412A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.728A= MANE Select ENSP00000302620.3:p.Asp243=
ENST00000307503.3:c.728A= ENSP00000302620.3:p.Asp243=
ENST00000476698.1:n.380A=
NM_000030.2:c.728A= NP_000021.1:p.Asp243=
NM_000030.3:c.728A= MANE Select NP_000021.1:p.Asp243=