Canonical Allele Identifier: CA2580068026
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 1725601
ClinVar RCV Id: RCV002309285

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869283del , CM000664.2:g.240869283del GRCh38
NC_000002.11:g.241808700del , CM000664.1:g.241808700del GRCh37
NC_000002.10:g.241457373del NCBI36
NG_008005.1:g.5539del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.279del MANE Select ENSP00000302620.3:p.Leu94TrpfsTer26
ENST00000307503.3:c.279del ENSP00000302620.3:p.Leu94TrpfsTer26
ENST00000472436.1:n.299del
NM_000030.2:c.279del NP_000021.1:p.Leu94TrpfsTer26
XR_924060.1:n.405+950del
NM_000030.3:c.279del MANE Select NP_000021.1:p.Leu94TrpfsTer26