Canonical Allele Identifier: CA1339335438

Gene: AGXT

Linked Data

• dbSNP Id: rs2059031596

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240877431del , CM000664.2:g.240877431del	GRCh38
NC_000002.11:g.241816848del , CM000664.1:g.241816848del	GRCh37
NC_000002.10:g.241465521del	NCBI36
NG_008005.1:g.13687del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.4:c.847-106del MANE Select	ENSP00000302620.3:n.847-106del
ENST00000307503.3:c.847-106del	ENSP00000302620.3:n.847-106del
ENST00000470255.1:n.519del
NM_000030.2:c.847-106del	NP_000021.1:n.847-106del
NM_000030.3:c.847-106del MANE Select	NP_000021.1:n.847-106del