Canonical Allele Identifier: CA68173644
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs796863670

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869100_240869102delinsGA , CM000664.2:g.240869100_240869102delinsGA GRCh38
NC_000002.11:g.241808517_241808519delinsGA , CM000664.1:g.241808517_241808519delinsGA GRCh37
NC_000002.10:g.241457190_241457192delinsGA NCBI36
NG_008005.1:g.5356_5358delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.166-70_166-68delinsGA MANE Select ENSP00000302620.3:n.166-70_166-68delinsGA...
ENST00000307503.3:c.166-70_166-68delinsGA ENSP00000302620.3:n.166-70_166-68delinsGA...
ENST00000472436.1:n.186-70_186-68delinsGA
NM_000030.2:c.166-70_166-68delinsGA NP_000021.1:n.166-70_166-68delinsGA
XR_924060.1:n.405+1131_405+1133delinsTC
NM_000030.3:c.166-70_166-68delinsGA MANE Select NP_000021.1:n.166-70_166-68delinsGA