Canonical Allele Identifier: CA1339335295
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877163_240877165delinsGGA , CM000664.2:g.240877163_240877165delinsGGA GRCh38
NC_000002.11:g.241816580_241816582delinsGGA , CM000664.1:g.241816580_241816582delinsGGA GRCh37
NC_000002.10:g.241465253_241465255delinsGGA NCBI36
NG_008005.1:g.13419_13421delinsGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.847-374_847-372delinsGGA MANE Select ENSP00000302620.3:n.847-374_847-372delinsGGA
ENST00000307503.3:c.847-374_847-372delinsGGA ENSP00000302620.3:n.847-374_847-372delinsGGA
ENST00000470255.1:n.251_253delinsGGA
NM_000030.2:c.847-374_847-372delinsGGA NP_000021.1:n.847-374_847-372delinsGGA
NM_000030.3:c.847-374_847-372delinsGGA MANE Select NP_000021.1:n.847-374_847-372delinsGGA