Canonical Allele Identifier: CA1339334214
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875198C= , CM000664.2:g.240875198C= GRCh38
NC_000002.11:g.241814615C= , CM000664.1:g.241814615C= GRCh37
NC_000002.10:g.241463288C= NCBI36
NG_008005.1:g.11454C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.770C= MANE Select ENSP00000302620.3:p.Pro257=
ENST00000307503.3:c.770C= ENSP00000302620.3:p.Pro257=
ENST00000476698.1:n.422C=
NM_000030.2:c.770C= NP_000021.1:p.Pro257=
NM_000030.3:c.770C= MANE Select NP_000021.1:p.Pro257=