Canonical Allele Identifier: CA1339330831
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869049_240869050delinsCG , CM000664.2:g.240869049_240869050delinsCG GRCh38
NC_000002.11:g.241808466_241808467delinsCG , CM000664.1:g.241808466_241808467delinsCG GRCh37
NC_000002.10:g.241457139_241457140delinsCG NCBI36
NG_008005.1:g.5305_5306delinsCG

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.165+19_165+20delinsCG MANE Select ENSP00000302620.3:n.165+19_165+20delinsCG...
ENST00000307503.3:c.165+19_165+20delinsCG ENSP00000302620.3:n.165+19_165+20delinsCG...
ENST00000472436.1:n.185+19_185+20delinsCG
NM_000030.2:c.165+19_165+20delinsCG NP_000021.1:n.165+19_165+20delinsCG
XR_924060.1:n.405+1183_405+1184delinsCG
NM_000030.3:c.165+19_165+20delinsCG MANE Select NP_000021.1:n.165+19_165+20delinsCG