Canonical Allele Identifier: CA2664006454
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240873401-A-AG
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873403dup , CM000664.2:g.240873403dup GRCh38
NC_000002.11:g.241812820dup , CM000664.1:g.241812820dup GRCh37
NC_000002.10:g.241461493dup NCBI36
NG_008005.1:g.9659dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.595+354dup MANE Select ENSP00000302620.3:n.595+354dup
ENST00000307503.3:c.595+354dup ENSP00000302620.3:n.595+354dup
ENST00000472436.1:n.969dup
ENST00000476698.1:n.332+354dup
NM_000030.2:c.595+354dup NP_000021.1:n.595+354dup
NM_000030.3:c.595+354dup MANE Select NP_000021.1:n.595+354dup
Search 100 bp 5'
Search 100 bp 3'