Canonical Allele Identifier: CA2664006189
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873324dup , CM000664.2:g.240873324dup GRCh38
NC_000002.11:g.241812741dup , CM000664.1:g.241812741dup GRCh37
NC_000002.10:g.241461414dup NCBI36
NG_008005.1:g.9580dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.595+275dup MANE Select ENSP00000302620.3:n.595+275dup
ENST00000307503.3:c.595+275dup ENSP00000302620.3:n.595+275dup
ENST00000472436.1:n.890dup
ENST00000476698.1:n.332+275dup
NM_000030.2:c.595+275dup NP_000021.1:n.595+275dup
NM_000030.3:c.595+275dup MANE Select NP_000021.1:n.595+275dup