Canonical Allele Identifier: CA2664007621

Gene: AGXT

Linked Data

• gnomAD v4: 2-240873948-A-ACCCGT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240873953_240873957dup , CM000664.2:g.240873953_240873957dup	GRCh38
NC_000002.11:g.241813370_241813374dup , CM000664.1:g.241813370_241813374dup	GRCh37
NC_000002.10:g.241462043_241462047dup	NCBI36
NG_008005.1:g.10209_10213dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.4:c.596-25_596-21dup MANE Select	ENSP00000302620.3:n.596-25_596-21dup
ENST00000307503.3:c.596-25_596-21dup	ENSP00000302620.3:n.596-25_596-21dup
ENST00000476698.1:n.332+904_332+908dup
NM_000030.2:c.596-25_596-21dup	NP_000021.1:n.596-25_596-21dup
NM_000030.3:c.596-25_596-21dup MANE Select	NP_000021.1:n.596-25_596-21dup