Canonical Allele Identifier: CA2673511902
Gene: AGXT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.34998652_34998653insATGTT , CM000667.2:g.34998652_34998653insATGTT GRCh38
NC_000005.9:g.34998757_34998758insATGTT , CM000667.1:g.34998757_34998758insATGTT GRCh37
NC_000005.8:g.35034514_35034515insATGTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000231420.11:c.*68_*69insCATAA MANE Select ENSP00000231420.6:n.*68_*69insCATAA
ENST00000231420.10:c.*68_*69insCATAA ENSP00000231420.6:n.*68_*69insCATAA
ENST00000510428.1:c.*45+23_*45+24insCATAA ENSP00000422799.1:n.*45+23_*45+24insCATAA
ENST00000512135.5:n.1283_1284insCATAA
ENST00000618015.4:c.*68_*69insCATAA ENSP00000479154.1:n.*68_*69insCATAA
NM_001306173.1:c.*45+23_*45+24insCATAA NP_001293102.1:n.*45+23_*45+24insCATAA
NM_031900.3:c.*68_*69insCATAA NP_114106.1:n.*68_*69insCATAA
XM_005248337.2:c.*68_*69insCATAA XP_005248394.1:n.*68_*69insCATAA
XM_005248338.2:c.*68_*69insCATAA XP_005248395.1:n.*68_*69insCATAA
XM_011514077.1:c.1438-249_1438-248insCATAA XP_011512379.1:n.1438-249_1438-248insCATAA
XM_005248337.3:c.*68_*69insCATAA XP_005248394.1:n.*68_*69insCATAA
XM_005248338.3:c.*68_*69insCATAA XP_005248395.1:n.*68_*69insCATAA
XM_017009748.2:c.*68_*69insCATAA XP_016865237.1:n.*68_*69insCATAA
NM_031900.4:c.*68_*69insCATAA MANE Select NP_114106.1:n.*68_*69insCATAA
NM_001306173.2:c.*45+23_*45+24insCATAA NP_001293102.1:n.*45+23_*45+24insCATAA