Canonical Allele Identifier: CA2695197708
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 2675047
ClinVar RCV Id: RCV003467925

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869272dup , CM000664.2:g.240869272dup GRCh38
NC_000002.11:g.241808689dup , CM000664.1:g.241808689dup GRCh37
NC_000002.10:g.241457362dup NCBI36
NG_008005.1:g.5528dup

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.268dup MANE Select ENSP00000302620.3:p.Leu90ProfsTer?
ENST00000307503.3:c.268dup ENSP00000302620.3:p.Leu90ProfsTer?
ENST00000472436.1:n.288dup
NM_000030.2:c.268dup NP_000021.1:p.Leu90ProfsTer?
XR_924060.1:n.405+963dup
NM_000030.3:c.268dup MANE Select NP_000021.1:p.Leu90ProfsTer?