Canonical Allele Identifier: CA2664006359

Gene: AGXT

Linked Data

• gnomAD v4: 2-240873381-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240873381_240873382insA , CM000664.2:g.240873381_240873382insA	GRCh38
NC_000002.11:g.241812798_241812799insA , CM000664.1:g.241812798_241812799insA	GRCh37
NC_000002.10:g.241461471_241461472insA	NCBI36
NG_008005.1:g.9637_9638insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.4:c.595+332_595+333insA MANE Select	ENSP00000302620.3:n.595+332_595+333insA
ENST00000307503.3:c.595+332_595+333insA	ENSP00000302620.3:n.595+332_595+333insA
ENST00000472436.1:n.947_948insA
ENST00000476698.1:n.332+332_332+333insA
NM_000030.2:c.595+332_595+333insA	NP_000021.1:n.595+332_595+333insA
NM_000030.3:c.595+332_595+333insA MANE Select	NP_000021.1:n.595+332_595+333insA