Canonical Allele Identifier: CA2664006014
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873214del , CM000664.2:g.240873214del GRCh38
NC_000002.11:g.241812631del , CM000664.1:g.241812631del GRCh37
NC_000002.10:g.241461304del NCBI36
NG_008005.1:g.9470del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.595+165del MANE Select ENSP00000302620.3:n.595+165del
ENST00000307503.3:c.595+165del ENSP00000302620.3:n.595+165del
ENST00000472436.1:n.780del
ENST00000476698.1:n.332+165del
NM_000030.2:c.595+165del NP_000021.1:n.595+165del
NM_000030.3:c.595+165del MANE Select NP_000021.1:n.595+165del