Canonical Allele Identifier: CA2664005077
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869083_240869084insCGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCAATCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCAC , CM000664.2:g.240869083_240869084insCGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCAATCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCAC GRCh38
NC_000002.11:g.241808500_241808501insCGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCAATCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCAC , CM000664.1:g.241808500_241808501insCGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCAATCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCAC GRCh37
NC_000002.10:g.241457173_241457174insCGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCAATCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCAC NCBI36
NG_008005.1:g.5339_5340insCGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCAATCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCAC

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.165+53_165+54insCGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCAATCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCAC MANE Select ENSP00000302620.3:n.165+53_165+54insCGATC...
ENST00000307503.3:c.165+53_165+54insCGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCAATCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCAC ENSP00000302620.3:n.165+53_165+54insCGATC...
ENST00000472436.1:n.185+53_185+54insCGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCAATCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCAC
NM_000030.2:c.165+53_165+54insCGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCAATCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCAC NP_000021.1:n.165+53_165+54insCGATCGTGGAC...
XR_924060.1:n.405+1158_405+1159insTACAGGGGTGAGACCCAGGCCCCCCGATTGAGGAAGCAGTGACCCCCTTCCCTCGTCCACGATCGGTGGGTGGG
NM_000030.3:c.165+53_165+54insCGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCAATCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCAC MANE Select NP_000021.1:n.165+53_165+54insCGATCGTGGAC...