Canonical Allele Identifier: CA1339336262
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879009C= , CM000664.2:g.240879009C= GRCh38
NC_000002.11:g.241818426C= , CM000664.1:g.241818426C= GRCh37
NC_000002.10:g.241467099C= NCBI36
NG_008005.1:g.15265C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*188C= MANE Select ENSP00000302620.3:n.*188C=
ENST00000307503.3:c.*188C= ENSP00000302620.3:n.*188C=
ENST00000470255.1:n.1145C=
NM_000030.2:c.*188C= NP_000021.1:n.*188C=
NM_000030.3:c.*188C= MANE Select NP_000021.1:n.*188C=