Canonical Allele Identifier: CA2664009247
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875349del , CM000664.2:g.240875349del GRCh38
NC_000002.11:g.241814766del , CM000664.1:g.241814766del GRCh37
NC_000002.10:g.241463439del NCBI36
NG_008005.1:g.11605del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.776+145del MANE Select ENSP00000302620.3:n.776+145del
ENST00000307503.3:c.776+145del ENSP00000302620.3:n.776+145del
ENST00000476698.1:n.428+145del
NM_000030.2:c.776+145del NP_000021.1:n.776+145del
NM_000030.3:c.776+145del MANE Select NP_000021.1:n.776+145del