Canonical Allele Identifier: CA2664005130
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869089_240869090insAGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCG , CM000664.2:g.240869089_240869090insAGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCG GRCh38
NC_000002.11:g.241808506_241808507insAGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCG , CM000664.1:g.241808506_241808507insAGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCG GRCh37
NC_000002.10:g.241457179_241457180insAGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCG NCBI36
NG_008005.1:g.5345_5346insAGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCG

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.165+59_165+60insAGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCG MANE Select ENSP00000302620.3:n.165+59_165+60insAGGAC...
ENST00000307503.3:c.165+59_165+60insAGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCG ENSP00000302620.3:n.165+59_165+60insAGGAC...
ENST00000472436.1:n.185+59_185+60insAGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCG
NM_000030.2:c.165+59_165+60insAGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCG NP_000021.1:n.165+59_165+60insAGGACGAGGGA...
XR_924060.1:n.405+1158_405+1159insTACAGGGGTGAGACCCAGGCCCCCCGAGTGAGGAAGCAGTGACCCCCTTCCCTCGTCCTCGATCTGTGGGTGGG
NM_000030.3:c.165+59_165+60insAGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCG MANE Select NP_000021.1:n.165+59_165+60insAGGACGAGGGA...