Canonical Allele Identifier: CA1339333269
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873392_240873393delinsAC , CM000664.2:g.240873392_240873393delinsAC GRCh38
NC_000002.11:g.241812809_241812810delinsAC , CM000664.1:g.241812809_241812810delinsAC GRCh37
NC_000002.10:g.241461482_241461483delinsAC NCBI36
NG_008005.1:g.9648_9649delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.595+343_595+344delinsAC MANE Select ENSP00000302620.3:n.595+343_595+344delinsAC
ENST00000307503.3:c.595+343_595+344delinsAC ENSP00000302620.3:n.595+343_595+344delinsAC
ENST00000472436.1:n.958_959delinsAC
ENST00000476698.1:n.332+343_332+344delinsAC
NM_000030.2:c.595+343_595+344delinsAC NP_000021.1:n.595+343_595+344delinsAC
NM_000030.3:c.595+343_595+344delinsAC MANE Select NP_000021.1:n.595+343_595+344delinsAC