Canonical Allele Identifier: CA2664012868
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240878867-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878870del , CM000664.2:g.240878870del GRCh38
NC_000002.11:g.241818287del , CM000664.1:g.241818287del GRCh37
NC_000002.10:g.241466960del NCBI36
NG_008005.1:g.15126del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*49del MANE Select ENSP00000302620.3:n.*49del
ENST00000307503.3:c.*49del ENSP00000302620.3:n.*49del
ENST00000470255.1:n.1006del
NM_000030.2:c.*49del NP_000021.1:n.*49del
NM_000030.3:c.*49del MANE Select NP_000021.1:n.*49del
Search 100 bp 5'
Search 100 bp 3'