Canonical Allele Identifier: CA1339335855
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878210_240878211delinsCA , CM000664.2:g.240878210_240878211delinsCA GRCh38
NC_000002.11:g.241817627_241817628delinsCA , CM000664.1:g.241817627_241817628delinsCA GRCh37
NC_000002.10:g.241466300_241466301delinsCA NCBI36
NG_008005.1:g.14466_14467delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.1071+60_1071+61delinsCA MANE Select ENSP00000302620.3:n.1071+60_1071+61delinsCA
ENST00000307503.3:c.1071+60_1071+61delinsCA ENSP00000302620.3:n.1071+60_1071+61delinsCA
ENST00000470255.1:n.849+60_849+61delinsCA
NM_000030.2:c.1071+60_1071+61delinsCA NP_000021.1:n.1071+60_1071+61delinsCA
NM_000030.3:c.1071+60_1071+61delinsCA MANE Select NP_000021.1:n.1071+60_1071+61delinsCA