Canonical Allele Identifier: CA2664005084
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869085_240869086insCTCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAG , CM000664.2:g.240869085_240869086insCTCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAG GRCh38
NC_000002.11:g.241808502_241808503insCTCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAG , CM000664.1:g.241808502_241808503insCTCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAG GRCh37
NC_000002.10:g.241457175_241457176insCTCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAG NCBI36
NG_008005.1:g.5341_5342insCTCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACCCACAG

Transcript Alleles

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