Canonical Allele Identifier: CA2664013146
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240878987-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878991del , CM000664.2:g.240878991del GRCh38
NC_000002.11:g.241818408del , CM000664.1:g.241818408del GRCh37
NC_000002.10:g.241467081del NCBI36
NG_008005.1:g.15247del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*170del MANE Select ENSP00000302620.3:n.*170del
ENST00000307503.3:c.*170del ENSP00000302620.3:n.*170del
ENST00000470255.1:n.1127del
NM_000030.2:c.*170del NP_000021.1:n.*170del
NM_000030.3:c.*170del MANE Select NP_000021.1:n.*170del
Search 100 bp 5'
Search 100 bp 3'