Canonical Allele Identifier: CA2664012028
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878174del , CM000664.2:g.240878174del GRCh38
NC_000002.11:g.241817591del , CM000664.1:g.241817591del GRCh37
NC_000002.10:g.241466264del NCBI36
NG_008005.1:g.14430del

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.1071+24del MANE Select ENSP00000302620.3:n.1071+24del
ENST00000307503.3:c.1071+24del ENSP00000302620.3:n.1071+24del
ENST00000470255.1:n.849+24del
NM_000030.2:c.1071+24del NP_000021.1:n.1071+24del
NM_000030.3:c.1071+24del MANE Select NP_000021.1:n.1071+24del