Canonical Allele Identifier: CA915940274
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 2681187
ClinVar RCV Id: RCV003468712

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875161_240875162del , CM000664.2:g.240875161_240875162del GRCh38
NC_000002.11:g.241814578_241814579del , CM000664.1:g.241814578_241814579del GRCh37
NC_000002.10:g.241463251_241463252del NCBI36
NG_008005.1:g.11417_11418del

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.733_734del MANE Select ENSP00000302620.3:p.Lys245ValfsTer9
ENST00000307503.3:c.733_734del ENSP00000302620.3:p.Lys245ValfsTer9
ENST00000476698.1:n.385_386del
NM_000030.2:c.733_734del NP_000021.1:p.Lys245ValfsTer9
NM_000030.3:c.733_734del MANE Select NP_000021.1:p.Lys245ValfsTer9