Canonical Allele Identifier: CA1339330862

Gene: AGXT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240869089_240869090delinsGT , CM000664.2:g.240869089_240869090delinsGT	GRCh38
NC_000002.11:g.241808506_241808507delinsGT , CM000664.1:g.241808506_241808507delinsGT	GRCh37
NC_000002.10:g.241457179_241457180delinsGT	NCBI36
NG_008005.1:g.5345_5346delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.4:c.165+59_165+60delinsGT MANE Select	ENSP00000302620.3:n.165+59_165+60delinsGT
ENST00000307503.3:c.165+59_165+60delinsGT	ENSP00000302620.3:n.165+59_165+60delinsGT
ENST00000472436.1:n.185+59_185+60delinsGT
NM_000030.2:c.165+59_165+60delinsGT	NP_000021.1:n.165+59_165+60delinsGT
XR_924060.1:n.405+1143_405+1144delinsAC
NM_000030.3:c.165+59_165+60delinsGT MANE Select	NP_000021.1:n.165+59_165+60delinsGT