Canonical Allele Identifier: CA2664005132
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869088_240869089insACGGAAGAGGGGAGGGGTCACTGCTTCCTCACTCTGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATC , CM000664.2:g.240869088_240869089insACGGAAGAGGGGAGGGGTCACTGCTTCCTCACTCTGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATC GRCh38
NC_000002.11:g.241808505_241808506insACGGAAGAGGGGAGGGGTCACTGCTTCCTCACTCTGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATC , CM000664.1:g.241808505_241808506insACGGAAGAGGGGAGGGGTCACTGCTTCCTCACTCTGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATC GRCh37
NC_000002.10:g.241457178_241457179insACGGAAGAGGGGAGGGGTCACTGCTTCCTCACTCTGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATC NCBI36
NG_008005.1:g.5344_5345insACGGAAGAGGGGAGGGGTCACTGCTTCCTCACTCTGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATC

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.165+58_165+59insACGGAAGAGGGGAGGGGTCACTGCTTCCTCACTCTGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATC MANE Select ENSP00000302620.3:n.165+58_165+59insACGGAAGAGGGGAGGGGTCACTGCT...
ENST00000307503.3:c.165+58_165+59insACGGAAGAGGGGAGGGGTCACTGCTTCCTCACTCTGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATC ENSP00000302620.3:n.165+58_165+59insACGGAAGAGGGGAGGGGTCACTGCT...
ENST00000472436.1:n.185+58_185+59insACGGAAGAGGGGAGGGGTCACTGCTTCCTCACTCTGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATC
NM_000030.2:c.165+58_165+59insACGGAAGAGGGGAGGGGTCACTGCTTCCTCACTCTGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATC NP_000021.1:n.165+58_165+59insACGGAAGAGGGGAGGGGTCACTGCTTCCTCA...
XR_924060.1:n.405+1158_405+1159insTACAGGGGTGAGACCCAGGCCCCCAGAGTGAGGAAGCAGTGACCCCTCCCCTCTTCCGTGATCTGTGGGTGGG
NM_000030.3:c.165+58_165+59insACGGAAGAGGGGAGGGGTCACTGCTTCCTCACTCTGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATC MANE Select NP_000021.1:n.165+58_165+59insACGGAAGAGGGGAGGGGTCACTGCTTCCTCA...