Canonical Allele Identifier: CA1339330978
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869287G= , CM000664.2:g.240869287G= GRCh38
NC_000002.11:g.241808704G= , CM000664.1:g.241808704G= GRCh37
NC_000002.10:g.241457377G= NCBI36
NG_008005.1:g.5543G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.283G= MANE Select ENSP00000302620.3:p.Glu95=
ENST00000307503.3:c.283G= ENSP00000302620.3:p.Glu95=
ENST00000472436.1:n.303G=
NM_000030.2:c.283G= NP_000021.1:p.Glu95=
XR_924060.1:n.405+946C=
NM_000030.3:c.283G= MANE Select NP_000021.1:p.Glu95=