Canonical Allele Identifier: CA1339332108
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240871408C= , CM000664.2:g.240871408C= GRCh38
NC_000002.11:g.241810825C= , CM000664.1:g.241810825C= GRCh37
NC_000002.10:g.241459498C= NCBI36
NG_008005.1:g.7664C=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.483C= MANE Select ENSP00000302620.3:p.Gly161=
ENST00000307503.3:c.483C= ENSP00000302620.3:p.Gly161=
ENST00000472436.1:n.503C=
ENST00000476698.1:n.220C=
NM_000030.2:c.483C= NP_000021.1:p.Gly161=
NM_000030.3:c.483C= MANE Select NP_000021.1:p.Gly161=