Canonical Allele Identifier: CA1339334180
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875138C= , CM000664.2:g.240875138C= GRCh38
NC_000002.11:g.241814555C= , CM000664.1:g.241814555C= GRCh37
NC_000002.10:g.241463228C= NCBI36
NG_008005.1:g.11394C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.710C= MANE Select ENSP00000302620.3:p.Pro237=
ENST00000307503.3:c.710C= ENSP00000302620.3:p.Pro237=
ENST00000476698.1:n.362C=
NM_000030.2:c.710C= NP_000021.1:p.Pro237=
NM_000030.3:c.710C= MANE Select NP_000021.1:p.Pro237=