Canonical Allele Identifier: CA2664010278
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877093del , CM000664.2:g.240877093del GRCh38
NC_000002.11:g.241816510del , CM000664.1:g.241816510del GRCh37
NC_000002.10:g.241465183del NCBI36
NG_008005.1:g.13349del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.847-444del MANE Select ENSP00000302620.3:n.847-444del
ENST00000307503.3:c.847-444del ENSP00000302620.3:n.847-444del
ENST00000470255.1:n.181del
NM_000030.2:c.847-444del NP_000021.1:n.847-444del
NM_000030.3:c.847-444del MANE Select NP_000021.1:n.847-444del