Canonical Allele Identifier: CA2664005141
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869074_240869075insACCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTA , CM000664.2:g.240869074_240869075insACCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTA GRCh38
NC_000002.11:g.241808491_241808492insACCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTA , CM000664.1:g.241808491_241808492insACCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTA GRCh37
NC_000002.10:g.241457164_241457165insACCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTA NCBI36
NG_008005.1:g.5330_5331insACCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTA

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.165+44_165+45insACCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTA MANE Select ENSP00000302620.3:n.165+44_165+45insACCAC...
ENST00000307503.3:c.165+44_165+45insACCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTA ENSP00000302620.3:n.165+44_165+45insACCAC...
ENST00000472436.1:n.185+44_185+45insACCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTA
NM_000030.2:c.165+44_165+45insACCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTA NP_000021.1:n.165+44_165+45insACCACCCACAG...
XR_924060.1:n.405+1158_405+1159insTACAGGGGTGAGACCCAGGCCCCCCGAGTGAGGAAGCAGTGACCCCCTTCCCTCGTCCACGATCTGTGGGTGGT
NM_000030.3:c.165+44_165+45insACCACCCACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTA MANE Select NP_000021.1:n.165+44_165+45insACCACCCACAG...