Canonical Allele Identifier: CA2499215816
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 1075767
ClinVar RCV Id: RCV001389457
dbSNP Id: rs2106430919

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875990del , CM000664.2:g.240875990del GRCh38
NC_000002.11:g.241815407del , CM000664.1:g.241815407del GRCh37
NC_000002.10:g.241464080del NCBI36
NG_008005.1:g.12246del

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.832del MANE Select ENSP00000302620.3:p.Leu278SerfsTer?
ENST00000307503.3:c.832del ENSP00000302620.3:p.Leu278SerfsTer?
ENST00000476698.1:n.484del
NM_000030.2:c.832del NP_000021.1:p.Leu278SerfsTer?
NM_000030.3:c.832del MANE Select NP_000021.1:p.Leu278SerfsTer?