Canonical Allele Identifier: CA2664005111
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869103_240869104insTGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGG , CM000664.2:g.240869103_240869104insTGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGG GRCh38
NC_000002.11:g.241808520_241808521insTGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGG , CM000664.1:g.241808520_241808521insTGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGG GRCh37
NC_000002.10:g.241457193_241457194insTGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGG NCBI36
NG_008005.1:g.5359_5360insTGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAGATCGTGGACGAGGGAAGG

Transcript Alleles

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