Canonical Allele Identifier: CA1339334261
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875296_240875303delinsGCCCCCCA , CM000664.2:g.240875296_240875303delinsGCCCCCCA GRCh38
NC_000002.11:g.241814713_241814720delinsGCCCCCCA , CM000664.1:g.241814713_241814720delinsGCCCCCCA GRCh37
NC_000002.10:g.241463386_241463393delinsGCCCCCCA NCBI36
NG_008005.1:g.11552_11559delinsGCCCCCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.776+92_776+99delinsGCCCCCCA MANE Select ENSP00000302620.3:n.776+92_776+99delinsGCCCCCCA
ENST00000307503.3:c.776+92_776+99delinsGCCCCCCA ENSP00000302620.3:n.776+92_776+99delinsGCCCCCCA
ENST00000476698.1:n.428+92_428+99delinsGCCCCCCA
NM_000030.2:c.776+92_776+99delinsGCCCCCCA NP_000021.1:n.776+92_776+99delinsGCCCCCCA
NM_000030.3:c.776+92_776+99delinsGCCCCCCA MANE Select NP_000021.1:n.776+92_776+99delinsGCCCCCCA