Canonical Allele Identifier: CA1339333083
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873030C= , CM000664.2:g.240873030C= GRCh38
NC_000002.11:g.241812447C= , CM000664.1:g.241812447C= GRCh37
NC_000002.10:g.241461120C= NCBI36
NG_008005.1:g.9286C=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.576C= MANE Select ENSP00000302620.3:p.Pro192=
ENST00000307503.3:c.576C= ENSP00000302620.3:p.Pro192=
ENST00000472436.1:n.596C=
ENST00000476698.1:n.313C=
NM_000030.2:c.576C= NP_000021.1:p.Pro192=
NM_000030.3:c.576C= MANE Select NP_000021.1:p.Pro192=