Canonical Allele Identifier: CA2664013954
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879197del , CM000664.2:g.240879197del GRCh38
NC_000002.11:g.241818614del , CM000664.1:g.241818614del GRCh37
NC_000002.10:g.241467287del NCBI36
NG_008005.1:g.15453del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*376del MANE Select ENSP00000302620.3:n.*376del
ENST00000470255.1:n.1333del
NM_000030.3:c.*376del MANE Select NP_000021.1:n.*376del