Canonical Allele Identifier: CA1339335856

Gene: AGXT

Linked Data

• dbSNP Id: rs2059038958
• gnomAD v4: 2-240878210-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240878211del , CM000664.2:g.240878211del	GRCh38
NC_000002.11:g.241817628del , CM000664.1:g.241817628del	GRCh37
NC_000002.10:g.241466301del	NCBI36
NG_008005.1:g.14467del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.4:c.1071+61del MANE Select	ENSP00000302620.3:n.1071+61del
ENST00000307503.3:c.1071+61del	ENSP00000302620.3:n.1071+61del
ENST00000470255.1:n.849+61del
NM_000030.2:c.1071+61del	NP_000021.1:n.1071+61del
NM_000030.3:c.1071+61del MANE Select	NP_000021.1:n.1071+61del