Canonical Allele Identifier: CA2701851369
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs2106431424

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877103del , CM000664.2:g.240877103del GRCh38
NC_000002.11:g.241816520del , CM000664.1:g.241816520del GRCh37
NC_000002.10:g.241465193del NCBI36
NG_008005.1:g.13359del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.847-434del MANE Select ENSP00000302620.3:n.847-434del
ENST00000307503.3:c.847-434del ENSP00000302620.3:n.847-434del
ENST00000470255.1:n.191del
NM_000030.2:c.847-434del NP_000021.1:n.847-434del
NM_000030.3:c.847-434del MANE Select NP_000021.1:n.847-434del