Canonical Allele Identifier: CA1339335519
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877572_240877575delinsCGCG , CM000664.2:g.240877572_240877575delinsCGCG GRCh38
NC_000002.11:g.241816989_241816992delinsCGCG , CM000664.1:g.241816989_241816992delinsCGCG GRCh37
NC_000002.10:g.241465662_241465665delinsCGCG NCBI36
NG_008005.1:g.13828_13831delinsCGCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.882_885delinsCGCG MANE Select ENSP00000302620.3:p.Ala294=
ENST00000307503.3:c.882_885delinsCGCG ENSP00000302620.3:p.Ala294=
ENST00000470255.1:n.660_663delinsCGCG
NM_000030.2:c.882_885delinsCGCG NP_000021.1:p.Ala294=
NM_000030.3:c.882_885delinsCGCG MANE Select NP_000021.1:p.Ala294=
Search 100 bp 5'
Search 100 bp 3'