Canonical Allele Identifier: CA2664006543
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869471_240869472insGGAA , CM000664.2:g.240869471_240869472insGGAA GRCh38
NC_000002.11:g.241808888_241808889insGGAA , CM000664.1:g.241808888_241808889insGGAA GRCh37
NC_000002.10:g.241457561_241457562insGGAA NCBI36
NG_008005.1:g.5727_5728insGGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.358+109_358+110insGGAA MANE Select ENSP00000302620.3:n.358+109_358+110insGGAA
ENST00000307503.3:c.358+109_358+110insGGAA ENSP00000302620.3:n.358+109_358+110insGGAA
ENST00000472436.1:n.378+109_378+110insGGAA
NM_000030.2:c.358+109_358+110insGGAA NP_000021.1:n.358+109_358+110insGGAA
XR_924060.1:n.405+762_405+763insTCCT
NM_000030.3:c.358+109_358+110insGGAA MANE Select NP_000021.1:n.358+109_358+110insGGAA