Canonical Allele Identifier: CA2664005919
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873142dup , CM000664.2:g.240873142dup GRCh38
NC_000002.11:g.241812559dup , CM000664.1:g.241812559dup GRCh37
NC_000002.10:g.241461232dup NCBI36
NG_008005.1:g.9398dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.595+93dup MANE Select ENSP00000302620.3:n.595+93dup
ENST00000307503.3:c.595+93dup ENSP00000302620.3:n.595+93dup
ENST00000472436.1:n.708dup
ENST00000476698.1:n.332+93dup
NM_000030.2:c.595+93dup NP_000021.1:n.595+93dup
NM_000030.3:c.595+93dup MANE Select NP_000021.1:n.595+93dup