Canonical Allele Identifier: CA2664005137
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869086_240869087insCCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGA , CM000664.2:g.240869086_240869087insCCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGA GRCh38
NC_000002.11:g.241808503_241808504insCCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGA , CM000664.1:g.241808503_241808504insCCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGA GRCh37
NC_000002.10:g.241457176_241457177insCCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGA NCBI36
NG_008005.1:g.5342_5343insCCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGA

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.165+56_165+57insCCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGA MANE Select ENSP00000302620.3:n.165+56_165+57insCCGTG...
ENST00000307503.3:c.165+56_165+57insCCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGA ENSP00000302620.3:n.165+56_165+57insCCGTG...
ENST00000472436.1:n.185+56_185+57insCCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGA
NM_000030.2:c.165+56_165+57insCCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGA NP_000021.1:n.165+56_165+57insCCGTGGACGAG...
XR_924060.1:n.405+1158_405+1159insTACAGGGGTGAGACCCAGGCCCCCCGAGTGAGGAAGCAGTGACCCCCTTCCCTCGTCCACGGTCTGTGGGTGGG
NM_000030.3:c.165+56_165+57insCCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGA MANE Select NP_000021.1:n.165+56_165+57insCCGTGGACGAG...