Canonical Allele Identifier: CA1339336299
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879081C= , CM000664.2:g.240879081C= GRCh38
NC_000002.11:g.241818498C= , CM000664.1:g.241818498C= GRCh37
NC_000002.10:g.241467171C= NCBI36
NG_008005.1:g.15337C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*260C= MANE Select ENSP00000302620.3:n.*260C=
ENST00000307503.3:c.*260C= ENSP00000302620.3:n.*260C=
ENST00000470255.1:n.1217C=
NM_000030.2:c.*260C= NP_000021.1:n.*260C=
NM_000030.3:c.*260C= MANE Select NP_000021.1:n.*260C=