Canonical Allele Identifier: CA1339336175
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878806C= , CM000664.2:g.240878806C= GRCh38
NC_000002.11:g.241818223C= , CM000664.1:g.241818223C= GRCh37
NC_000002.10:g.241466896C= NCBI36
NG_008005.1:g.15062C=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.1164C= MANE Select ENSP00000302620.3:p.Pro388=
ENST00000307503.3:c.1164C= ENSP00000302620.3:p.Pro388=
ENST00000470255.1:n.942C=
NM_000030.2:c.1164C= NP_000021.1:p.Pro388=
NM_000030.3:c.1164C= MANE Select NP_000021.1:p.Pro388=