Canonical Allele Identifier: CA2664007537
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873911del , CM000664.2:g.240873911del GRCh38
NC_000002.11:g.241813328del , CM000664.1:g.241813328del GRCh37
NC_000002.10:g.241462001del NCBI36
NG_008005.1:g.10167del

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.596-67del MANE Select ENSP00000302620.3:n.596-67del
ENST00000307503.3:c.596-67del ENSP00000302620.3:n.596-67del
ENST00000476698.1:n.332+862del
NM_000030.2:c.596-67del NP_000021.1:n.596-67del
NM_000030.3:c.596-67del MANE Select NP_000021.1:n.596-67del