Canonical Allele Identifier: CA2664005078
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869085_240869086insTTCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAG , CM000664.2:g.240869085_240869086insTTCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAG GRCh38
NC_000002.11:g.241808502_241808503insTTCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAG , CM000664.1:g.241808502_241808503insTTCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAG GRCh37
NC_000002.10:g.241457175_241457176insTTCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAG NCBI36
NG_008005.1:g.5341_5342insTTCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAG

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.165+55_165+56insTTCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAG MANE Select ENSP00000302620.3:n.165+55_165+56insTTCGT...
ENST00000307503.3:c.165+55_165+56insTTCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAG ENSP00000302620.3:n.165+55_165+56insTTCGT...
ENST00000472436.1:n.185+55_185+56insTTCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAG
NM_000030.2:c.165+55_165+56insTTCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAG NP_000021.1:n.165+55_165+56insTTCGTGGACGA...
XR_924060.1:n.405+1158_405+1159insTACAGGGGTGAGACCCAGGCCCCCCGAGTGAGGAAGCAGTGACCCCCTTCCCTCGTCCACGAACTGTGGGTGGG
NM_000030.3:c.165+55_165+56insTTCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAG MANE Select NP_000021.1:n.165+55_165+56insTTCGTGGACGA...