Canonical Allele Identifier: CA2664011049
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877483del , CM000664.2:g.240877483del GRCh38
NC_000002.11:g.241816900del , CM000664.1:g.241816900del GRCh37
NC_000002.10:g.241465573del NCBI36
NG_008005.1:g.13739del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.847-54del MANE Select ENSP00000302620.3:n.847-54del
ENST00000307503.3:c.847-54del ENSP00000302620.3:n.847-54del
ENST00000470255.1:n.571del
NM_000030.2:c.847-54del NP_000021.1:n.847-54del
NM_000030.3:c.847-54del MANE Select NP_000021.1:n.847-54del