Canonical Allele Identifier: CA1339330884
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869116_240869144delinsCCTCACTTGGGGAGGCGGGGAGCCTGGGT , CM000664.2:g.240869116_240869144delinsCCTCACTTGGGGAGGCGGGGAGCCTGGGT GRCh38
NC_000002.11:g.241808533_241808561delinsCCTCACTTGGGGAGGCGGGGAGCCTGGGT , CM000664.1:g.241808533_241808561delinsCCTCACTTGGGGAGGCGGGGAGCCTGGGT GRCh37
NC_000002.10:g.241457206_241457234delinsCCTCACTTGGGGAGGCGGGGAGCCTGGGT NCBI36
NG_008005.1:g.5372_5400delinsCCTCACTTGGGGAGGCGGGGAGCCTGGGT

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.166-54_166-26delinsCCTCACTTGGGGAGGCGGGGAGCCTGGGT MANE Select ENSP00000302620.3:n.166-54_166-26delinsCC...
ENST00000307503.3:c.166-54_166-26delinsCCTCACTTGGGGAGGCGGGGAGCCTGGGT ENSP00000302620.3:n.166-54_166-26delinsCC...
ENST00000472436.1:n.186-54_186-26delinsCCTCACTTGGGGAGGCGGGGAGCCTGGGT
NM_000030.2:c.166-54_166-26delinsCCTCACTTGGGGAGGCGGGGAGCCTGGGT NP_000021.1:n.166-54_166-26delinsCCTCACTT...
XR_924060.1:n.405+1089_405+1117delinsACCCAGGCTCCCCGCCTCCCCAAGTGAGG
NM_000030.3:c.166-54_166-26delinsCCTCACTTGGGGAGGCGGGGAGCCTGGGT MANE Select NP_000021.1:n.166-54_166-26delinsCCTCACTT...