Canonical Allele Identifier: CA1339336336
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs2059044318

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879172_240879180del , CM000664.2:g.240879172_240879180del GRCh38
NC_000002.11:g.241818589_241818597del , CM000664.1:g.241818589_241818597del GRCh37
NC_000002.10:g.241467262_241467270del NCBI36
NG_008005.1:g.15428_15436del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*351_*359del MANE Select ENSP00000302620.3:n.*351_*359del
ENST00000470255.1:n.1308_1316del
NM_000030.3:c.*351_*359del MANE Select NP_000021.1:n.*351_*359del