Canonical Allele Identifier: CA2664006350
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873383dup , CM000664.2:g.240873383dup GRCh38
NC_000002.11:g.241812800dup , CM000664.1:g.241812800dup GRCh37
NC_000002.10:g.241461473dup NCBI36
NG_008005.1:g.9639dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.595+334dup MANE Select ENSP00000302620.3:n.595+334dup
ENST00000307503.3:c.595+334dup ENSP00000302620.3:n.595+334dup
ENST00000472436.1:n.949dup
ENST00000476698.1:n.332+334dup
NM_000030.2:c.595+334dup NP_000021.1:n.595+334dup
NM_000030.3:c.595+334dup MANE Select NP_000021.1:n.595+334dup