Canonical Allele Identifier: CA1339330926
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869178C= , CM000664.2:g.240869178C= GRCh38
NC_000002.11:g.241808595C= , CM000664.1:g.241808595C= GRCh37
NC_000002.10:g.241457268C= NCBI36
NG_008005.1:g.5434C=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.174C= MANE Select ENSP00000302620.3:p.Asp58=
ENST00000307503.3:c.174C= ENSP00000302620.3:p.Asp58=
ENST00000472436.1:n.194C=
NM_000030.2:c.174C= NP_000021.1:p.Asp58=
XR_924060.1:n.405+1055G=
NM_000030.3:c.174C= MANE Select NP_000021.1:p.Asp58=