Canonical Allele Identifier: CA2664011564

Gene: AGXT

Linked Data

• gnomAD v4: 2-240877915-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240877917dup , CM000664.2:g.240877917dup	GRCh38
NC_000002.11:g.241817334dup , CM000664.1:g.241817334dup	GRCh37
NC_000002.10:g.241466007dup	NCBI36
NG_008005.1:g.14173dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.4:c.943-105dup MANE Select	ENSP00000302620.3:n.943-105dup
ENST00000307503.3:c.943-105dup	ENSP00000302620.3:n.943-105dup
ENST00000470255.1:n.721-105dup
NM_000030.2:c.943-105dup	NP_000021.1:n.943-105dup
NM_000030.3:c.943-105dup MANE Select	NP_000021.1:n.943-105dup