Canonical Allele Identifier: CA2664005096
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869096_240869097insTGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGA , CM000664.2:g.240869096_240869097insTGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGA GRCh38
NC_000002.11:g.241808513_241808514insTGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGA , CM000664.1:g.241808513_241808514insTGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGA GRCh37
NC_000002.10:g.241457186_241457187insTGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGA NCBI36
NG_008005.1:g.5352_5353insTGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGA

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.165+66_165+67insTGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGA MANE Select ENSP00000302620.3:n.165+66_165+67insTGGAA...
ENST00000307503.3:c.165+66_165+67insTGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGA ENSP00000302620.3:n.165+66_165+67insTGGAA...
ENST00000472436.1:n.185+66_185+67insTGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGA
NM_000030.2:c.165+66_165+67insTGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGA NP_000021.1:n.165+66_165+67insTGGAAGGGGGT...
XR_924060.1:n.405+1158_405+1159insTACAGGGGTGAGACCCAGGCCCCCCGAGTGAGGAAGCAGTGACCCCCTTCCATCGTCCACGATCTGTGGGTGGG
NM_000030.3:c.165+66_165+67insTGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGA MANE Select NP_000021.1:n.165+66_165+67insTGGAAGGGGGT...