Canonical Allele Identifier: CA2664010830
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877354_240877358del , CM000664.2:g.240877354_240877358del GRCh38
NC_000002.11:g.241816771_241816775del , CM000664.1:g.241816771_241816775del GRCh37
NC_000002.10:g.241465444_241465448del NCBI36
NG_008005.1:g.13610_13614del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.847-183_847-179del MANE Select ENSP00000302620.3:n.847-183_847-179del
ENST00000307503.3:c.847-183_847-179del ENSP00000302620.3:n.847-183_847-179del
ENST00000470255.1:n.442_446del
NM_000030.2:c.847-183_847-179del NP_000021.1:n.847-183_847-179del
NM_000030.3:c.847-183_847-179del MANE Select NP_000021.1:n.847-183_847-179del