Canonical Allele Identifier: CA2754892480
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879053_240879054insT , CM000664.2:g.240879053_240879054insT GRCh38
NC_000002.11:g.241818470_241818471insT , CM000664.1:g.241818470_241818471insT GRCh37
NC_000002.10:g.241467143_241467144insT NCBI36
NG_008005.1:g.15309_15310insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*232_*233insT MANE Select ENSP00000302620.3:n.*232_*233insT
ENST00000307503.3:c.*232_*233insT ENSP00000302620.3:n.*232_*233insT
ENST00000470255.1:n.1189_1190insT
NM_000030.2:c.*232_*233insT NP_000021.1:n.*232_*233insT
NM_000030.3:c.*232_*233insT MANE Select NP_000021.1:n.*232_*233insT