Canonical Allele Identifier: CA1339335496
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877535_240877536delinsAG , CM000664.2:g.240877535_240877536delinsAG GRCh38
NC_000002.11:g.241816952_241816953delinsAG , CM000664.1:g.241816952_241816953delinsAG GRCh37
NC_000002.10:g.241465625_241465626delinsAG NCBI36
NG_008005.1:g.13791_13792delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.847-2_847-1delinsAG MANE Select ENSP00000302620.3:n.847-2_847-1delinsAG
ENST00000307503.3:c.847-2_847-1delinsAG ENSP00000302620.3:n.847-2_847-1delinsAG
ENST00000470255.1:n.623_624delinsAG
NM_000030.2:c.847-2_847-1delinsAG NP_000021.1:n.847-2_847-1delinsAG
NM_000030.3:c.847-2_847-1delinsAG MANE Select NP_000021.1:n.847-2_847-1delinsAG