Canonical Allele Identifier: CA2577302209
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 2664110
ClinVar RCV Id: RCV003445256

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869228del , CM000664.2:g.240869228del GRCh38
NC_000002.11:g.241808645del , CM000664.1:g.241808645del GRCh37
NC_000002.10:g.241457318del NCBI36
NG_008005.1:g.5484del

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.224del MANE Select ENSP00000302620.3:p.Thr75AsnfsTer?
ENST00000307503.3:c.224del ENSP00000302620.3:p.Thr75AsnfsTer?
ENST00000472436.1:n.244del
NM_000030.2:c.224del NP_000021.1:p.Thr75AsnfsTer?
XR_924060.1:n.405+1005del
NM_000030.3:c.224del MANE Select NP_000021.1:p.Thr75AsnfsTer?