Canonical Allele Identifier: CA2522336334
Gene: AGXT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.34998690_34998691insACTCCATT , CM000667.2:g.34998690_34998691insACTCCATT GRCh38
NC_000005.9:g.34998795_34998796insACTCCATT , CM000667.1:g.34998795_34998796insACTCCATT GRCh37
NC_000005.8:g.35034552_35034553insACTCCATT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000231420.11:c.*28_*29insAATGGAGT MANE Select ENSP00000231420.6:n.*28_*29insAATGGAGT
ENST00000231420.10:c.*28_*29insAATGGAGT ENSP00000231420.6:n.*28_*29insAATGGAGT
ENST00000510428.1:c.*28_*29insAATGGAGT ENSP00000422799.1:n.*28_*29insAATGGAGT
ENST00000512135.5:n.1243_1244insAATGGAGT
ENST00000618015.4:c.*28_*29insAATGGAGT ENSP00000479154.1:n.*28_*29insAATGGAGT
NM_001306173.1:c.*28_*29insAATGGAGT NP_001293102.1:n.*28_*29insAATGGAGT
NM_031900.3:c.*28_*29insAATGGAGT NP_114106.1:n.*28_*29insAATGGAGT
XM_005248337.2:c.*28_*29insAATGGAGT XP_005248394.1:n.*28_*29insAATGGAGT
XM_005248338.2:c.*28_*29insAATGGAGT XP_005248395.1:n.*28_*29insAATGGAGT
XM_011514077.1:c.1438-289_1438-288insAATGGAGT XP_011512379.1:n.1438-289_1438-288insAATGGAGT
XM_005248337.3:c.*28_*29insAATGGAGT XP_005248394.1:n.*28_*29insAATGGAGT
XM_005248338.3:c.*28_*29insAATGGAGT XP_005248395.1:n.*28_*29insAATGGAGT
XM_017009748.2:c.*28_*29insAATGGAGT XP_016865237.1:n.*28_*29insAATGGAGT
NM_031900.4:c.*28_*29insAATGGAGT MANE Select NP_114106.1:n.*28_*29insAATGGAGT
NM_001306173.2:c.*28_*29insAATGGAGT NP_001293102.1:n.*28_*29insAATGGAGT