Canonical Allele Identifier: CA1044064792
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869079_240869080insTCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCAC , CM000664.2:g.240869079_240869080insTCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCAC GRCh38
NC_000002.11:g.241808496_241808497insTCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCAC , CM000664.1:g.241808496_241808497insTCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCAC GRCh37
NC_000002.10:g.241457169_241457170insTCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCAC NCBI36
NG_008005.1:g.5335_5336insTCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCAC

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.165+49_165+50insTCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCAC MANE Select ENSP00000302620.3:n.165+49_165+50insTCACA...
ENST00000307503.3:c.165+49_165+50insTCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCAC ENSP00000302620.3:n.165+49_165+50insTCACA...
ENST00000472436.1:n.185+49_185+50insTCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCAC
NM_000030.2:c.165+49_165+50insTCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCAC NP_000021.1:n.165+49_165+50insTCACAGATCGT...
XR_924060.1:n.405+1158_405+1159insTACAGGGGTGAGACCCAGGCCCCCCGAGTGAGGAAGCAGTGACCCCCTTCCCTCGTCCACGATCTGTGAGTGGG
NM_000030.3:c.165+49_165+50insTCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCAC MANE Select NP_000021.1:n.165+49_165+50insTCACAGATCGT...