Canonical Allele Identifier: CA2664009252

Gene: AGXT

Linked Data

• gnomAD v4: 2-240875351-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240875351_240875352insG , CM000664.2:g.240875351_240875352insG	GRCh38
NC_000002.11:g.241814768_241814769insG , CM000664.1:g.241814768_241814769insG	GRCh37
NC_000002.10:g.241463441_241463442insG	NCBI36
NG_008005.1:g.11607_11608insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.4:c.776+147_776+148insG MANE Select	ENSP00000302620.3:n.776+147_776+148insG
ENST00000307503.3:c.776+147_776+148insG	ENSP00000302620.3:n.776+147_776+148insG
ENST00000476698.1:n.428+147_428+148insG
NM_000030.2:c.776+147_776+148insG	NP_000021.1:n.776+147_776+148insG
NM_000030.3:c.776+147_776+148insG MANE Select	NP_000021.1:n.776+147_776+148insG