Canonical Allele Identifier: CA2664005139
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869080_240869081insAACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACC , CM000664.2:g.240869080_240869081insAACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACC GRCh38
NC_000002.11:g.241808497_241808498insAACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACC , CM000664.1:g.241808497_241808498insAACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACC GRCh37
NC_000002.10:g.241457170_241457171insAACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACC NCBI36
NG_008005.1:g.5336_5337insAACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACC

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.165+50_165+51insAACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACC MANE Select ENSP00000302620.3:n.165+50_165+51insAACAG...
ENST00000307503.3:c.165+50_165+51insAACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACC ENSP00000302620.3:n.165+50_165+51insAACAG...
ENST00000472436.1:n.185+50_185+51insAACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACC
NM_000030.2:c.165+50_165+51insAACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACC NP_000021.1:n.165+50_165+51insAACAGATCGTG...
XR_924060.1:n.405+1158_405+1159insTACAGGGGTGAGACCCAGGCCCCCCGAGTGAGGAAGCAGTGACCCCCTTCCCTCGTCCACGATCTGTTGGTGGG
NM_000030.3:c.165+50_165+51insAACAGATCGTGGACGAGGGAAGGGGGTCACTGCTTCCTCACTCGGGGGGCCTGGGTCTCACCCCTGTACCCACC MANE Select NP_000021.1:n.165+50_165+51insAACAGATCGTG...