Canonical Allele Identifier: CA1339336291
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879064C= , CM000664.2:g.240879064C= GRCh38
NC_000002.11:g.241818481C= , CM000664.1:g.241818481C= GRCh37
NC_000002.10:g.241467154C= NCBI36
NG_008005.1:g.15320C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*243C= MANE Select ENSP00000302620.3:n.*243C=
ENST00000307503.3:c.*243C= ENSP00000302620.3:n.*243C=
ENST00000470255.1:n.1200C=
NM_000030.2:c.*243C= NP_000021.1:n.*243C=
NM_000030.3:c.*243C= MANE Select NP_000021.1:n.*243C=