Canonical Allele Identifier: CA2664005198
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869098_240869099insCAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGG , CM000664.2:g.240869098_240869099insCAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGG GRCh38
NC_000002.11:g.241808515_241808516insCAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGG , CM000664.1:g.241808515_241808516insCAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGG GRCh37
NC_000002.10:g.241457188_241457189insCAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGG NCBI36
NG_008005.1:g.5354_5355insCAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGG

Transcript Alleles

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