Canonical Allele Identifier: CA2664006341

Gene: AGXT

Linked Data

• gnomAD v4: 2-240873377-GC-G

Genomic Alleles

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

Transcript Alleles

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