Canonical Allele Identifier: CA2664006271
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240873359-CA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873360del , CM000664.2:g.240873360del GRCh38
NC_000002.11:g.241812777del , CM000664.1:g.241812777del GRCh37
NC_000002.10:g.241461450del NCBI36
NG_008005.1:g.9616del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.595+311del MANE Select ENSP00000302620.3:n.595+311del
ENST00000307503.3:c.595+311del ENSP00000302620.3:n.595+311del
ENST00000472436.1:n.926del
ENST00000476698.1:n.332+311del
NM_000030.2:c.595+311del NP_000021.1:n.595+311del
NM_000030.3:c.595+311del MANE Select NP_000021.1:n.595+311del
Search 100 bp 5'
Search 100 bp 3'