Canonical Allele Identifier: CA2664013953
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240879192-A-AT
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879192_240879193insT , CM000664.2:g.240879192_240879193insT GRCh38
NC_000002.11:g.241818609_241818610insT , CM000664.1:g.241818609_241818610insT GRCh37
NC_000002.10:g.241467282_241467283insT NCBI36
NG_008005.1:g.15448_15449insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*371_*372insT MANE Select ENSP00000302620.3:n.*371_*372insT
ENST00000470255.1:n.1328_1329insT
NM_000030.3:c.*371_*372insT MANE Select NP_000021.1:n.*371_*372insT
Search 100 bp 5'
Search 100 bp 3'