Canonical Allele Identifier: CA2664008859

Gene: AGXT

Linked Data

• gnomAD v4: 2-240875097-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240875100del , CM000664.2:g.240875100del	GRCh38
NC_000002.11:g.241814517del , CM000664.1:g.241814517del	GRCh37
NC_000002.10:g.241463190del	NCBI36
NG_008005.1:g.11356del

Transcript Alleles

HGVS	Amino-acid change
ENST00000307503.4:c.681-9del MANE Select	ENSP00000302620.3:n.681-9del
ENST00000307503.3:c.681-9del	ENSP00000302620.3:n.681-9del
ENST00000476698.1:n.333-9del
NM_000030.2:c.681-9del	NP_000021.1:n.681-9del
NM_000030.3:c.681-9del MANE Select	NP_000021.1:n.681-9del