Canonical Allele Identifier: CA2664005116
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869098_240869099insAAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGG , CM000664.2:g.240869098_240869099insAAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGG GRCh38
NC_000002.11:g.241808515_241808516insAAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGG , CM000664.1:g.241808515_241808516insAAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGG GRCh37
NC_000002.10:g.241457188_241457189insAAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGG NCBI36
NG_008005.1:g.5354_5355insAAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGG

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.165+68_165+69insAAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGG MANE Select ENSP00000302620.3:n.165+68_165+69insAAAGG...
ENST00000307503.3:c.165+68_165+69insAAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGG ENSP00000302620.3:n.165+68_165+69insAAAGG...
ENST00000472436.1:n.185+68_185+69insAAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGG
NM_000030.2:c.165+68_165+69insAAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGG NP_000021.1:n.165+68_165+69insAAAGGGGGTCA...
XR_924060.1:n.405+1158_405+1159insTACAGGGGTGAGACCCAGGCCCCCCGAGTGAGGAAGCAGTGACCCCCTTTCCTCGTCCACGATCTGTGGGTGGG
NM_000030.3:c.165+68_165+69insAAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGG MANE Select NP_000021.1:n.165+68_165+69insAAAGGGGGTCA...