Canonical Allele Identifier: CA2664010852
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877362_240877364del , CM000664.2:g.240877362_240877364del GRCh38
NC_000002.11:g.241816779_241816781del , CM000664.1:g.241816779_241816781del GRCh37
NC_000002.10:g.241465452_241465454del NCBI36
NG_008005.1:g.13618_13620del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.847-175_847-173del MANE Select ENSP00000302620.3:n.847-175_847-173del
ENST00000307503.3:c.847-175_847-173del ENSP00000302620.3:n.847-175_847-173del
ENST00000470255.1:n.450_452del
NM_000030.2:c.847-175_847-173del NP_000021.1:n.847-175_847-173del
NM_000030.3:c.847-175_847-173del MANE Select NP_000021.1:n.847-175_847-173del