Canonical Allele Identifier: CA2664012979
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240878938-AC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878941del , CM000664.2:g.240878941del GRCh38
NC_000002.11:g.241818358del , CM000664.1:g.241818358del GRCh37
NC_000002.10:g.241467031del NCBI36
NG_008005.1:g.15197del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*120del MANE Select ENSP00000302620.3:n.*120del
ENST00000307503.3:c.*120del ENSP00000302620.3:n.*120del
ENST00000470255.1:n.1077del
NM_000030.2:c.*120del NP_000021.1:n.*120del
NM_000030.3:c.*120del MANE Select NP_000021.1:n.*120del
Search 100 bp 5'
Search 100 bp 3'