Canonical Allele Identifier: CA2754892253
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873268_240873269insAC , CM000664.2:g.240873268_240873269insAC GRCh38
NC_000002.11:g.241812685_241812686insAC , CM000664.1:g.241812685_241812686insAC GRCh37
NC_000002.10:g.241461358_241461359insAC NCBI36
NG_008005.1:g.9524_9525insAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.595+219_595+220insAC MANE Select ENSP00000302620.3:n.595+219_595+220insAC
ENST00000307503.3:c.595+219_595+220insAC ENSP00000302620.3:n.595+219_595+220insAC
ENST00000472436.1:n.834_835insAC
ENST00000476698.1:n.332+219_332+220insAC
NM_000030.2:c.595+219_595+220insAC NP_000021.1:n.595+219_595+220insAC
NM_000030.3:c.595+219_595+220insAC MANE Select NP_000021.1:n.595+219_595+220insAC