Canonical Allele Identifier: CA2664006222
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873346del , CM000664.2:g.240873346del GRCh38
NC_000002.11:g.241812763del , CM000664.1:g.241812763del GRCh37
NC_000002.10:g.241461436del NCBI36
NG_008005.1:g.9602del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.595+297del MANE Select ENSP00000302620.3:n.595+297del
ENST00000307503.3:c.595+297del ENSP00000302620.3:n.595+297del
ENST00000472436.1:n.912del
ENST00000476698.1:n.332+297del
NM_000030.2:c.595+297del NP_000021.1:n.595+297del
NM_000030.3:c.595+297del MANE Select NP_000021.1:n.595+297del