Canonical Allele Identifier: CA2832544654
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873407_240873411del , CM000664.2:g.240873407_240873411del GRCh38
NC_000002.11:g.241812824_241812828del , CM000664.1:g.241812824_241812828del GRCh37
NC_000002.10:g.241461497_241461501del NCBI36
NG_008005.1:g.9663_9667del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.595+358_595+362del MANE Select ENSP00000302620.3:n.595+358_595+362del
ENST00000307503.3:c.595+358_595+362del ENSP00000302620.3:n.595+358_595+362del
ENST00000472436.1:n.973_977del
ENST00000476698.1:n.332+358_332+362del
NM_000030.2:c.595+358_595+362del NP_000021.1:n.595+358_595+362del
NM_000030.3:c.595+358_595+362del MANE Select NP_000021.1:n.595+358_595+362del