Canonical Allele Identifier: CA2664006344

Gene: AGXT

Linked Data

• gnomAD v4: 2-240873378-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240873378_240873379insG , CM000664.2:g.240873378_240873379insG	GRCh38
NC_000002.11:g.241812795_241812796insG , CM000664.1:g.241812795_241812796insG	GRCh37
NC_000002.10:g.241461468_241461469insG	NCBI36
NG_008005.1:g.9634_9635insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.4:c.595+329_595+330insG MANE Select	ENSP00000302620.3:n.595+329_595+330insG
ENST00000307503.3:c.595+329_595+330insG	ENSP00000302620.3:n.595+329_595+330insG
ENST00000472436.1:n.944_945insG
ENST00000476698.1:n.332+329_332+330insG
NM_000030.2:c.595+329_595+330insG	NP_000021.1:n.595+329_595+330insG
NM_000030.3:c.595+329_595+330insG MANE Select	NP_000021.1:n.595+329_595+330insG