Canonical Allele Identifier: CA2664005195
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869103_240869104insAGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGG , CM000664.2:g.240869103_240869104insAGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGG GRCh38
NC_000002.11:g.241808520_241808521insAGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGG , CM000664.1:g.241808520_241808521insAGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGG GRCh37
NC_000002.10:g.241457193_241457194insAGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGG NCBI36
NG_008005.1:g.5359_5360insAGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGG

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.166-67_166-66insAGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGG MANE Select ENSP00000302620.3:n.166-67_166-66insAGGTC...
ENST00000307503.3:c.166-67_166-66insAGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGG ENSP00000302620.3:n.166-67_166-66insAGGTC...
ENST00000472436.1:n.186-67_186-66insAGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGG
NM_000030.2:c.166-67_166-66insAGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGG NP_000021.1:n.166-67_166-66insAGGTCACTGCT...
XR_924060.1:n.405+1158_405+1159insTACAGGGGTGAGACCCAGGCCCCCCGAGTGAGGAAGCAGTGACCTCCTTCCCTCGTCCACGATCTGTGGGTGGG
NM_000030.3:c.166-67_166-66insAGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGG MANE Select NP_000021.1:n.166-67_166-66insAGGTCACTGCT...