Canonical Allele Identifier: CA1339336322
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879138_240879140delinsGAA , CM000664.2:g.240879138_240879140delinsGAA GRCh38
NC_000002.11:g.241818555_241818557delinsGAA , CM000664.1:g.241818555_241818557delinsGAA GRCh37
NC_000002.10:g.241467228_241467230delinsGAA NCBI36
NG_008005.1:g.15394_15396delinsGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*317_*319delinsGAA MANE Select ENSP00000302620.3:n.*317_*319delinsGAA
ENST00000470255.1:n.1274_1276delinsGAA
NM_000030.3:c.*317_*319delinsGAA MANE Select NP_000021.1:n.*317_*319delinsGAA