Canonical Allele Identifier: CA1339334193
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875160C= , CM000664.2:g.240875160C= GRCh38
NC_000002.11:g.241814577C= , CM000664.1:g.241814577C= GRCh37
NC_000002.10:g.241463250C= NCBI36
NG_008005.1:g.11416C=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.732C= MANE Select ENSP00000302620.3:p.Ile244=
ENST00000307503.3:c.732C= ENSP00000302620.3:p.Ile244=
ENST00000476698.1:n.384C=
NM_000030.2:c.732C= NP_000021.1:p.Ile244=
NM_000030.3:c.732C= MANE Select NP_000021.1:p.Ile244=