Canonical Allele Identifier: CA2664010286

Gene: AGXT

Linked Data

• gnomAD v4: 2-240877094-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240877094_240877095insG , CM000664.2:g.240877094_240877095insG	GRCh38
NC_000002.11:g.241816511_241816512insG , CM000664.1:g.241816511_241816512insG	GRCh37
NC_000002.10:g.241465184_241465185insG	NCBI36
NG_008005.1:g.13350_13351insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.4:c.847-443_847-442insG MANE Select	ENSP00000302620.3:n.847-443_847-442insG
ENST00000307503.3:c.847-443_847-442insG	ENSP00000302620.3:n.847-443_847-442insG
ENST00000470255.1:n.182_183insG
NM_000030.2:c.847-443_847-442insG	NP_000021.1:n.847-443_847-442insG
NM_000030.3:c.847-443_847-442insG MANE Select	NP_000021.1:n.847-443_847-442insG