Canonical Allele Identifier: CA2701856366
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs2106429848

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873943dup , CM000664.2:g.240873943dup GRCh38
NC_000002.11:g.241813360dup , CM000664.1:g.241813360dup GRCh37
NC_000002.10:g.241462033dup NCBI36
NG_008005.1:g.10199dup

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.596-35dup MANE Select ENSP00000302620.3:n.596-35dup
ENST00000307503.3:c.596-35dup ENSP00000302620.3:n.596-35dup
ENST00000476698.1:n.332+894dup
NM_000030.2:c.596-35dup NP_000021.1:n.596-35dup
NM_000030.3:c.596-35dup MANE Select NP_000021.1:n.596-35dup