Canonical Allele Identifier: CA2664013637
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240879112-TCTC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879116_240879118del , CM000664.2:g.240879116_240879118del GRCh38
NC_000002.11:g.241818533_241818535del , CM000664.1:g.241818533_241818535del GRCh37
NC_000002.10:g.241467206_241467208del NCBI36
NG_008005.1:g.15372_15374del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*295_*297del MANE Select ENSP00000302620.3:n.*295_*297del
ENST00000307503.3:c.*295_*297del ENSP00000302620.3:n.*295_*297del
ENST00000470255.1:n.1252_1254del
NM_000030.2:c.*295_*297del NP_000021.1:n.*295_*297del
NM_000030.3:c.*295_*297del MANE Select NP_000021.1:n.*295_*297del
Search 100 bp 5'
Search 100 bp 3'