Canonical Allele Identifier: CA2754891868
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868932_240868933insCAAACACACCCAACAC , CM000664.2:g.240868932_240868933insCAAACACACCCAACAC GRCh38
NC_000002.11:g.241808349_241808350insCAAACACACCCAACAC , CM000664.1:g.241808349_241808350insCAAACACACCCAACAC GRCh37
NC_000002.10:g.241457022_241457023insCAAACACACCCAACAC NCBI36
NG_008005.1:g.5188_5189insCAAACACACCCAACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.67_68insCAAACACACCCAACAC MANE Select ENSP00000302620.3:p.Gln23ProfsTer?
ENST00000307503.3:c.67_68insCAAACACACCCAACAC ENSP00000302620.3:p.Gln23ProfsTer?
ENST00000472436.1:n.87_88insCAAACACACCCAACAC
NM_000030.2:c.67_68insCAAACACACCCAACAC NP_000021.1:p.Gln23ProfsTer?
XR_924060.1:n.405+1301_405+1302insTGTTGGGTGTGTTTGG
NM_000030.3:c.67_68insCAAACACACCCAACAC MANE Select NP_000021.1:p.Gln23ProfsTer?